Cleared Traditional

K872991 - MICRINS FORCEPS 2010
(FDA 510(k) Clearance)

K872991 · Micrins Surgical, Inc. · General & Plastic Surgery device

Aug 1987

Decision

17d

Days

Class 1

Risk

K872991 is an FDA 510(k) clearance for the MICRINS FORCEPS 2010. This device is classified as a Forceps, General & Plastic Surgery (Class I - General Controls, product code GEN).

Submitted by Micrins Surgical, Inc. (Chicago, US). The FDA issued a Cleared decision on August 17, 1987, 17 days after receiving the submission on July 31, 1987.

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

Submission Details

510(k) Number	K872991 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	July 31, 1987
Decision Date	August 17, 1987
Days to Decision	17 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—