FDA 510(k)

SURGICAL RETRACTOR

K-Number: K760422 · 1976-08-23

Decision Date1976-08-23

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SURGICAL RETRACTOR 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 1976-08-23 under 510(k) number K760422. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL RETRACTOR?

SURGICAL RETRACTOR is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K760422.

When did SURGICAL RETRACTOR receive FDA 510(k) clearance?

SURGICAL RETRACTOR received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760422.

Who is the listed applicant for SURGICAL RETRACTOR?

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

What is the FDA product code for SURGICAL RETRACTOR?

The FDA product code for SURGICAL RETRACTOR is GAD.

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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.