Cleared Traditional

FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER

K944790 · Applied Medical Resources · General & Plastic Surgery
Nov 1994
Decision
62d
Days
Class 1
Risk

About This 510(k) Submission

K944790 is an FDA 510(k) clearance for the FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER, a Catheter, Cholangiography (Class I — General Controls, product code GBZ), submitted by Applied Medical Resources (Launa Hills, US). The FDA issued a Cleared decision on November 29, 1994, 62 days after receiving the submission on September 28, 1994. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4200.

Submission Details

510(k) Number K944790 FDA.gov
FDA Decision Cleared SESE
Date Received September 28, 1994
Decision Date November 29, 1994
Days to Decision 62 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GBZ — Catheter, Cholangiography
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4200

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