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FDA 510(k)

GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT

K-Number: K872326 · 1987-08-11

Decision Date1987-08-11
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT is the device name listed in this FDA 510(k) record. The listed applicant is Technology Management & Marketing, Inc.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K872326. The device is classified under product code JTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT?

GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is Technology Management & Marketing, Inc.. The 510(k) number is K872326.

When did GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT receive FDA 510(k) clearance?

GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872326.

Who is the listed applicant for GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT?

The FDA 510(k) record lists Technology Management & Marketing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT?

The FDA product code for GONOSTAT MALE SPECIMEN COLLECTION & TRANSPORT is JTW.

Related Clinical Trials

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.

Other records listing Technology Management & Marketing, Inc. 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.

Related Devices (Code: JTW)

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.

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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