GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT
K-Number: K872325 · 1987-08-12
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Device Summary
Frequently Asked Questions
What is the GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT?
GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is Technology Management & Marketing, Inc.. The 510(k) number is K872325.
When did GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT receive FDA 510(k) clearance?
GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT received FDA 510(k) clearance on 1987-08-12, under 510(k) number K872325.
Who is the listed applicant for GONOSTAT FEMALE 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 FEMALE SPECIMEN COLLECTION & TRANSPORT?
The FDA product code for GONOSTAT FEMALE 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
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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