Cleared Traditional

K823325 - DENTAL INSTRUMENTS - SURGICAL FORCEPS
(FDA 510(k) Clearance)

K823325 · Miltex, Inc. · Dental

Nov 1982

Decision

16d

Days

Class 1

Risk

K823325 is an FDA 510(k) clearance for the DENTAL INSTRUMENTS - SURGICAL FORCEPS. This device is classified as a Forceps, Tooth Extractor, Surgical (Class I — General Controls, product code EMG).

Submitted by Miltex, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 24, 1982, 16 days after receiving the submission on November 8, 1982.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.

Submission Details

510(k) Number	K823325 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 08, 1982
Decision Date	November 24, 1982
Days to Decision	16 days
Submission Type	Traditional
Review Panel	Dental (DE)
Summary	—