Cleared Traditional

METAL URETERAL BASKET STONE DISLODGER

K934675 · Annex Medical, Inc. · Gastroenterology & Urology
Jan 1994
Decision
101d
Days
Class 2
Risk

About This 510(k) Submission

K934675 is an FDA 510(k) clearance for the METAL URETERAL BASKET STONE DISLODGER, a Dislodger, Stone, Basket, Ureteral, Metal (Class II — Special Controls, product code FFL), submitted by Annex Medical, Inc. (Eden Prairie, US). The FDA issued a Cleared decision on January 7, 1994, 101 days after receiving the submission on September 28, 1993. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4680.

Submission Details

510(k) Number K934675 FDA.gov
FDA Decision Cleared SESE
Date Received September 28, 1993
Decision Date January 07, 1994
Days to Decision 101 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FFL — Dislodger, Stone, Basket, Ureteral, Metal
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.4680

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