Cleared Traditional

FORCEPS

K904723 · Minto Research & Development, Inc. · General & Plastic Surgery

Jul 1991

Decision

282d

Days

Class 1

Risk

About This 510(k) Submission

K904723 is an FDA 510(k) clearance for the FORCEPS, a Forceps, General & Plastic Surgery (Class I — General Controls, product code GEN), submitted by Minto Research & Development, Inc. (Redding, US). The FDA issued a Cleared decision on July 26, 1991, 282 days after receiving the submission on October 17, 1990. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4800.

Submission Details

510(k) Number	K904723 FDA.gov
FDA Decision	Cleared SESE
Date Received	October 17, 1990
Decision Date	July 26, 1991
Days to Decision	282 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—