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FDA 510(k)

LAPAROSCOPIC CURVED TRIANGLE RETRACTOR

K-Number: K922435 · 1992-12-24

Decision Date1992-12-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC CURVED TRIANGLE 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 1992-12-24 under 510(k) number K922435. 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 LAPAROSCOPIC CURVED TRIANGLE RETRACTOR?

LAPAROSCOPIC CURVED TRIANGLE RETRACTOR is a medical device that received FDA 510(k) clearance on 1992-12-24. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K922435.

When did LAPAROSCOPIC CURVED TRIANGLE RETRACTOR receive FDA 510(k) clearance?

LAPAROSCOPIC CURVED TRIANGLE RETRACTOR received FDA 510(k) clearance on 1992-12-24, under 510(k) number K922435.

Who is the listed applicant for LAPAROSCOPIC CURVED TRIANGLE 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 LAPAROSCOPIC CURVED TRIANGLE RETRACTOR?

The FDA product code for LAPAROSCOPIC CURVED TRIANGLE RETRACTOR is GCJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Advanced Surgical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 21 devices →

Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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