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FDA 510(k)

SURGICAL RETRACTOR

K-Number: K921287 · 1993-03-04

ApplicantAdvanced Surgical, Inc.
Decision Date1993-03-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGICAL RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K921287. The device is classified under product code GCJ. It was reviewed by the GU 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 1993-03-04. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K921287.

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

SURGICAL RETRACTOR received FDA 510(k) clearance on 1993-03-04, under 510(k) number K921287.

Who is the listed applicant for SURGICAL RETRACTOR?

The FDA 510(k) record lists Advanced Surgical, 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 GCJ.

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Other records listing Advanced Surgical, Inc. as applicant

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Related Devices (Code: GCJ)

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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.

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