Cleared Traditional

K821276 - MAYO SCISSOR CURYED 5 1/2
(FDA 510(k) Clearance)

K821276 · Conphar, Inc. · Dental

May 1982

Decision

25d

Days

Class 1

Risk

K821276 is an FDA 510(k) clearance for the MAYO SCISSOR CURYED 5 1/2. This device is classified as a Scissors, Surgical Tissue, Dental (Class I — General Controls, product code EGN).

Submitted by Conphar, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 28, 1982, 25 days after receiving the submission on May 3, 1982.

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

Submission Details

510(k) Number	K821276 FDA.gov
FDA Decision	Cleared SESE
Date Received	May 03, 1982
Decision Date	May 28, 1982
Days to Decision	25 days
Submission Type	Traditional
Review Panel	Dental (DE)
Summary	—