Cleared Traditional

K821277 - KELLY FORCEPS CURVED 5 1/2
(FDA 510(k) Clearance)

K821277 · Conphar, Inc. · General & Plastic Surgery device

May 1982

Decision

24d

Days

Class 1

Risk

K821277 is an FDA 510(k) clearance for the KELLY FORCEPS CURVED 5 1/2. 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	K821277 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (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	—