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FDA 510(k)

AUTO SUTURE SUTURE CLOSURE

K-Number: K954853 · 1995-12-20

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1995-12-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE SUTURE CLOSURE 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 1995-12-20 under 510(k) number K954853. 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 SUTURE CLOSURE?

AUTO SUTURE SUTURE CLOSURE is a medical device that received FDA 510(k) clearance on 1995-12-20. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K954853.

When did AUTO SUTURE SUTURE CLOSURE receive FDA 510(k) clearance?

AUTO SUTURE SUTURE CLOSURE received FDA 510(k) clearance on 1995-12-20, under 510(k) number K954853.

Who is the listed applicant for AUTO SUTURE SUTURE CLOSURE?

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 SUTURE CLOSURE?

The FDA product code for AUTO SUTURE SUTURE CLOSURE 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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