Cleared Traditional

K821280 - TISSUE FORCEPS
(FDA 510(k) Clearance)

K821280 · Conphar, Inc. · General & Plastic Surgery
May 1982
Decision
24d
Days
Class 1
Risk

K821280 is an FDA 510(k) clearance for the TISSUE FORCEPS. This device is classified as a Forceps, General & Plastic Surgery (Class I — General Controls, product code GEN).

Submitted by Conphar, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 27, 1982, 24 days after receiving the submission on May 3, 1982.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.

Submission Details

510(k) Number K821280 FDA.gov
FDA Decision Cleared SESE
Date Received May 03, 1982
Decision Date May 27, 1982
Days to Decision 24 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary —

Device Classification

Product Code GEN — Forceps, General & Plastic Surgery
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4800