K852302Substantially Equivalent

Inox Iorceps Jar

Name: K852302 Inox Iorceps Jar
Creator: Broadwest Corp.
Published: 1985-07-02
License: https://open.fda.gov/license/

Broadwest Corp., New York NY / Traditional, Substantially Equivalent

FDA source

K852302 is the FDA 510(k) clearance record for INOX IORCEPS JAR, cleared for Broadwest Corp. on 1985-07-02. FDA records list 6 510(k) clearances for Broadwest Corp., from 1985-05-09 to 1987-02-04. As of 2026-09-10, FDA records show no recalls naming K852302.

Clearance record

Decision date: 1985-07-02
Received: 1985-05-29 (34 days to decision)
Review panel: Unknown
Applicant: Broadwest Corp. 260 W. Broadway, New York NY
Third party review: No