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FDA 510(k)

QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150

K-Number: K982621 · 1998-10-16

ApplicantPhamatech
Decision Date1998-10-16
Product CodeMVO
DecisionSubstantially Equivalent

Device Summary

QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150 is the device name listed in this FDA 510(k) record. The listed applicant is Phamatech. It received FDA 510(k) clearance on 1998-10-16 under 510(k) number K982621. The device is classified under product code MVO. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150?

QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150 is a medical device that received FDA 510(k) clearance on 1998-10-16. The listed applicant is Phamatech. The 510(k) number is K982621.

When did QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150 receive FDA 510(k) clearance?

QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150 received FDA 510(k) clearance on 1998-10-16, under 510(k) number K982621.

Who is the listed applicant for QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150?

The FDA 510(k) record lists Phamatech as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150?

The FDA product code for QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150 is MVO.

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Other records listing Phamatech as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K041578QUICKSCREEN, MODELS 9177X AND 9178XK030447AT HOME DRUG CUP, MODEL 9150XK010833AT WORK DRUG TEST, MODEL 9177T AWTK010836AT WORK DRUG TEST, MODEL 9147T AWTK010653AT HOME DRUG TEST, MODEL 9068 TK010655AT HOME DRUG TESTT, MODEL 9150 T

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Related Devices (Code: MVO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K040327ACCU-STAT HOME DRUG TESTS FOR MARIJUANA (THC) AND FOR MARIJUANA & COCAINE (THC, COC)Accu-Stat Diagnostics, Inc.K030447AT HOME DRUG CUP, MODEL 9150XPhamatechK014192LIFESIGN MET, STATUS STIK MET, ACCUSIGN STIK MET, ACCUSTIK MET, ACCUSIGN MET, STATUS DS METPrinceton BioMeditech Corp.K013778PEACE OF MIND HOME DRUG TESTAdvantage Diagnostics Corp.K013409AT HOME DRUG TEST, MODEL 9074Phamatech, Inc.K013412AT HOME DRUG TEST, MODEL 9069Phamatech, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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