MODEL TR RECTAL SUCTION BIOPSY TUBE— 510(k) K902097

Name: FDA 510(k) clearance K902097
Creator: U.S. Food and Drug Administration
Published: 1990-07-27

Substantially Equivalent

Medical Measurements, Inc.

FDA 510(k) clearance K902097 for MODEL TR RECTAL SUCTION BIOPSY TUBE, Substantially Equivalent on 1990-07-27. Applicant: Medical Measurements, Inc.. Device class: 2.

Clearance details

Applicant: Medical Measurements, Inc.
Product code: Code FCK
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-08
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hackensack, NJ, US

Download summary PDF View on FDA.gov ↗

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