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FDA 510(k)

AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR

K-Number: K920068 · 1992-09-17

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1992-09-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR 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 1992-09-17 under 510(k) number K920068. 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 AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR?

AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR is a medical device that received FDA 510(k) clearance on 1992-09-17. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K920068.

When did AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR receive FDA 510(k) clearance?

AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR received FDA 510(k) clearance on 1992-09-17, under 510(k) number K920068.

Who is the listed applicant for AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR?

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 AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR?

The FDA product code for AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR is GCJ.

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Other records listing United States Surgical, A Division of Tyco Healthc 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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