FDA 510(k)

SUTURE GUIDE

K-Number: K760235 · 1976-07-26

Decision Date1976-07-26

Product Code

DecisionSubstantially Equivalent

Device Summary

SUTURE GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1976-07-26 under 510(k) number K760235. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE GUIDE?

SUTURE GUIDE is a medical device that received FDA 510(k) clearance on 1976-07-26. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K760235.

When did SUTURE GUIDE receive FDA 510(k) clearance?

SUTURE GUIDE received FDA 510(k) clearance on 1976-07-26, under 510(k) number K760235.

Who is the listed applicant for SUTURE GUIDE?

The FDA 510(k) record lists Cutter Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.