Cleared Traditional

UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT

K953787 · Unicor, Inc. · Anesthesiology

Sep 1995

Decision

36d

Days

Class 1

Risk

About This 510(k) Submission

K953787 is an FDA 510(k) clearance for the UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT, a Circuit, Breathing (w Connector, Adaptor, Y Piece) (Class I — General Controls, product code CAI), submitted by Unicor, Inc. (Cleveland, US). The FDA issued a Cleared decision on September 19, 1995, 36 days after receiving the submission on August 14, 1995. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5240.

Submission Details

510(k) Number	K953787 FDA.gov
FDA Decision	Cleared SESE
Date Received	August 14, 1995
Decision Date	September 19, 1995
Days to Decision	36 days
Submission Type	Traditional
Review Panel	Anesthesiology (AN)
Summary	Statement