Cleared Traditional

STOMA MEASURING DEVICE

K914482 · Biosearch Medical Products, Inc. · Gastroenterology & Urology
Dec 1991
Decision
80d
Days
Class 2
Risk

About This 510(k) Submission

K914482 is an FDA 510(k) clearance for the STOMA MEASURING DEVICE, a Tube, Feeding (Class II — Special Controls, product code FPD), submitted by Biosearch Medical Products, Inc. (Somerville, US). The FDA issued a Cleared decision on December 27, 1991, 80 days after receiving the submission on October 8, 1991. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K914482 FDA.gov
FDA Decision Cleared SESE
Date Received October 08, 1991
Decision Date December 27, 1991
Days to Decision 80 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FPD — Tube, Feeding
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5980

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