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FDA 510(k)

AUTO SUTURE SURGIWAND

K-Number: K961771 · 1996-09-25

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1996-09-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE SURGIWAND 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 1996-09-25 under 510(k) number K961771. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE SURGIWAND?

AUTO SUTURE SURGIWAND is a medical device that received FDA 510(k) clearance on 1996-09-25. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K961771.

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

AUTO SUTURE SURGIWAND received FDA 510(k) clearance on 1996-09-25, under 510(k) number K961771.

Who is the listed applicant for AUTO SUTURE SURGIWAND?

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 SURGIWAND?

The FDA product code for AUTO SUTURE SURGIWAND is GEI.

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

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Related Devices (Code: GEI)

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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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