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FDA 510(k)

THORACOSCOPE/LAPAROSCOPE

K-Number: K931954 · 1993-11-02

Decision Date1993-11-02
Product CodeGCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THORACOSCOPE/LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K931954. The device is classified under product code GCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORACOSCOPE/LAPAROSCOPE?

THORACOSCOPE/LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K931954.

When did THORACOSCOPE/LAPAROSCOPE receive FDA 510(k) clearance?

THORACOSCOPE/LAPAROSCOPE received FDA 510(k) clearance on 1993-11-02, under 510(k) number K931954.

Who is the listed applicant for THORACOSCOPE/LAPAROSCOPE?

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

What is the FDA product code for THORACOSCOPE/LAPAROSCOPE?

The FDA product code for THORACOSCOPE/LAPAROSCOPE is GCM.

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 Surgical Technologies, 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 28 devices →

Related Devices (Code: GCM)

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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