K760235Substantially Equivalent

Suture Guide

Name: K760235 Suture Guide
Creator: Cutter Laboratories, Inc.
Published: 1976-07-26
License: https://open.fda.gov/license/

Cutter Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K760235 is the FDA 510(k) clearance record for SUTURE GUIDE, cleared for Cutter Laboratories, Inc. on 1976-07-26. FDA records list 39 510(k) clearances for Cutter Laboratories, Inc., from 1976-07-26 to 1986-05-21. As of 2026-09-10, FDA records show no recalls naming K760235.

Clearance record

Decision date: 1976-07-26
Received: 1976-07-15 (11 days to decision)
Review panel: Unknown
Applicant: Cutter Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No