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FDA 510(k)

AUTO SUTURE POLY SURGICLIP HEMOSTATIC

K-Number: K831457 · 1983-08-08

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1983-08-08
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE POLY SURGICLIP HEMOSTATIC 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 1983-08-08 under 510(k) number K831457. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE POLY SURGICLIP HEMOSTATIC?

AUTO SUTURE POLY SURGICLIP HEMOSTATIC is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K831457.

When did AUTO SUTURE POLY SURGICLIP HEMOSTATIC receive FDA 510(k) clearance?

AUTO SUTURE POLY SURGICLIP HEMOSTATIC received FDA 510(k) clearance on 1983-08-08, under 510(k) number K831457.

Who is the listed applicant for AUTO SUTURE POLY SURGICLIP HEMOSTATIC?

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 POLY SURGICLIP HEMOSTATIC?

The FDA product code for AUTO SUTURE POLY SURGICLIP HEMOSTATIC is FZP.

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Related Devices (Code: FZP)

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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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