Cleared Traditional

K852857 - 4 X 4' GAUZE PAD
(FDA 510(k) Clearance)

K852857 · Cornelia Damsky, Inc. · General & Plastic Surgery

Jul 1985

Decision

21d

Days

—

Risk

K852857 is an FDA 510(k) clearance for the 4 X 4' GAUZE PAD. This device is classified as a Gauze/sponge, Internal.

Submitted by Cornelia Damsky, Inc. (Stamford, US). The FDA issued a Cleared decision on July 26, 1985, 21 days after receiving the submission on July 5, 1985.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number	K852857 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 05, 1985
Decision Date	July 26, 1985
Days to Decision	21 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—