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FDA 510(k)

MODEL TR RECTAL SUCTION BIOPSY TUBE

K-Number: K902097 · 1990-07-27

ApplicantMedical Measurements, Inc.
Decision Date1990-07-27
Product CodeFCK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL TR RECTAL SUCTION BIOPSY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Measurements, Inc.. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K902097. The device is classified under product code FCK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL TR RECTAL SUCTION BIOPSY TUBE?

MODEL TR RECTAL SUCTION BIOPSY TUBE is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K902097.

When did MODEL TR RECTAL SUCTION BIOPSY TUBE receive FDA 510(k) clearance?

MODEL TR RECTAL SUCTION BIOPSY TUBE received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902097.

Who is the listed applicant for MODEL TR RECTAL SUCTION BIOPSY TUBE?

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

What is the FDA product code for MODEL TR RECTAL SUCTION BIOPSY TUBE?

The FDA product code for MODEL TR RECTAL SUCTION BIOPSY TUBE is FCK.

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Other records listing Medical Measurements, 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.

K921062GAELTEC MPR SERIESK863479MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURALK801757MMI/GAELTEC CATHETER TIP PRESS. TRANSDUK801756MMI/GAELTEC CATHETER TIP TRANSDUCK801880MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANSK801758MMI/GAELTEC CATHETER INTRAUTERINE

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Related Devices (Code: FCK)

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.

K153763Howell Biliary Aspiration NeedleWilson-Cook Medical, Inc.K103326MULTIPLE BIOPSY SYSTEMUnited States Endoscopy Group, Inc.K062159RB12 SUCTION RECTAL BIOPSY SYSTEMAus Systems Pty , Ltd.K061201DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087United States Endoscopy Group, Inc.K051637DSNARE, MODEL 00711087United States Endoscopy Group, Inc.K954693MEHTA BRONCHIAL BIOSPY DRILLUnited States Endoscopy Group, 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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