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FDA 510(k)

AUTO SUTURE STAINLESS STEEL SUTURES*

K-Number: K872532 · 1987-08-05

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1987-08-05
Product CodeGAO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE STAINLESS STEEL SUTURES* 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 1987-08-05 under 510(k) number K872532. The device is classified under product code GAO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE STAINLESS STEEL SUTURES*?

AUTO SUTURE STAINLESS STEEL SUTURES* is a medical device that received FDA 510(k) clearance on 1987-08-05. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K872532.

When did AUTO SUTURE STAINLESS STEEL SUTURES* receive FDA 510(k) clearance?

AUTO SUTURE STAINLESS STEEL SUTURES* received FDA 510(k) clearance on 1987-08-05, under 510(k) number K872532.

Who is the listed applicant for AUTO SUTURE STAINLESS STEEL SUTURES*?

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 STAINLESS STEEL SUTURES*?

The FDA product code for AUTO SUTURE STAINLESS STEEL SUTURES* is GAO.

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

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Related Devices (Code: GAO)

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.

K932513LABELING FOR MYO/WIRE II STERNOTOMY SUTURESAlto Development Corp.K863034SHARPOINT STAINLESS STEEL SUTUREChathamborough Research Group, Inc.K802248DISARP ORIGINALUnoplast A/S

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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