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FDA 510(k)

ENDOSCOPE SUTURE & CARRIER

K-Number: K912973 · 1991-09-27

Decision Date1991-09-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE SUTURE & CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1991-09-27 under 510(k) number K912973. 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 ENDOSCOPE SUTURE & CARRIER?

ENDOSCOPE SUTURE & CARRIER is a medical device that received FDA 510(k) clearance on 1991-09-27. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K912973.

When did ENDOSCOPE SUTURE & CARRIER receive FDA 510(k) clearance?

ENDOSCOPE SUTURE & CARRIER received FDA 510(k) clearance on 1991-09-27, under 510(k) number K912973.

Who is the listed applicant for ENDOSCOPE SUTURE & CARRIER?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPE SUTURE & CARRIER?

The FDA product code for ENDOSCOPE SUTURE & CARRIER 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 United States Surgical, A Division of Tyco Healthc 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 218 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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