ILLNESSES & INJURIES

Name: Central Jersey Urgent Care
Price range: $

My InstaDoc Treats Non-Life Threatening Illnesses and Injuries in Children and Adults of All Ages

If you suspect that you or your loved is experiencing a life-threatening emergency, please call 911 or go to your nearest Emergency Room. In all other instances, My InstaDoc of Monroe is pleased to offer comprehensive care for all non-emergency conditions, including but not limited to the following:

Allergies and Allergic Reactions
Influenza (Flu)
(Common) Cold
Strep/Sore Throat
Infections
Ear Infections
Cuts and Minor Lacerations
Sprains and Strains
Fractures
Minor Joint Dislocations
Headaches
Sunburn
Minor and Moderate Burns
Rashes, Abscesses, and Boils

Get your latest COVID-19 and FLU/RSV Test Results

Please search for your test results in order to print them.

Testing Information

Your test was performed using one of the machines below:

Genesis Laboratory
Testing was performed using either of the following machines Thermo Fisher TaqMan 2019-nCoV Assay Kit v1, TaqMan 2019-nCoV Control Kit v1 Test, TaqPath COVID-19 Combo Kit and/ or Panther Fusion®️ SARS-CoV-2 Assay Kit. Positive results do not rule out co-infection with organisms not included in the Thermo Fisher TaqMan 2019-nCoV Assay Kit v1 and TaqMan 2019-nCoV Control Kit v1, TaqPath COVID-19 Combo Kit and/ or Panther Fusion®️ SARS-CoV-2 Assay Kit. The agent detected may not be the definite cause of this disease. This assay is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA). This test is only authorized for the duration of time of the declaration and for the detection of SARSCoV-2 RNS virus and/or diagnosis of COVID-19 infection under section 564 (b)(1) of the act, 21 U.S.C.360bbb-3(b)(1) unless the authorization is terminated or revoked sooner.
Clarity Laboratory
Virokey SARS CoV-2 real time PCR assay for detection of SARS CoV-2 from nasopharyngeal and oropharyngeal specimen was developed and its performance characteristics determined by Clarity Labs. The EUA approval #EU201790. This test is approved by CLIA, NJDOH and NYDOH. This test has been validated in accordance to FDA’s guidance document:”Policy for Diagnosis testing in laboratory verified to perform High complexity testing under CLIA prior to Emergency Use Authorization for Coronavirus disease-2019 during the public health emergency issued on February 29th 2020”. Negative results for symptomatic patients does not rule out the possibility of other bacterial or viral infections. Negative results does not rule out possibility of prior viral exposure. When Flag AB: Abnormal

NOTE: Results are uploaded each night, so if you don't see the results, try again tomorrow morning. If you have not found the test results after 5 days, please contact our office at (732) 781-0244 and select the office you tested.