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FDA 510(k)

V.D.T.-GONORRHEA TEST KIT

K-Number: K840799 · 1984-06-07

ApplicantM.G. Laboratories, Inc.
Decision Date1984-06-07
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

V.D.T.-GONORRHEA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is M.G. Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K840799. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V.D.T.-GONORRHEA TEST KIT?

V.D.T.-GONORRHEA TEST KIT is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is M.G. Laboratories, Inc.. The 510(k) number is K840799.

When did V.D.T.-GONORRHEA TEST KIT receive FDA 510(k) clearance?

V.D.T.-GONORRHEA TEST KIT received FDA 510(k) clearance on 1984-06-07, under 510(k) number K840799.

Who is the listed applicant for V.D.T.-GONORRHEA TEST KIT?

The FDA 510(k) record lists M.G. Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V.D.T.-GONORRHEA TEST KIT?

The FDA product code for V.D.T.-GONORRHEA TEST KIT is LIO.

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Related Devices (Code: LIO)

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.

K222613ARX Liquid Amies Collection & Transport SystemArx Sciences, Inc.K131630PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEMPuritan Medical Products, LLCK120846TRANSPORT CULTURE MEDIUM DEVICEPuritan Medical Products, LLCK103805MEDICAL WIRE & EQUIPMENT S-TRANSWAB (OR SIGMA-TRANSWAB) LIQUID AMIES COLLECTION AND TRANSPORT DEVICEMedical Wire & Equipment Company (Bath), Ltd.K082472VIROCULT, MODEL MW950Medical Wire & Equipment Company (Bath), Ltd.K070062COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USEDiesse Diagnostica Senese S.P.A.

Official Source

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

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