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FDA 510(k)

AUTO SUTURE TITANIUM HEMOSTATIC CLIP

K-Number: K853650 · 1985-09-19

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1985-09-19
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE TITANIUM HEMOSTATIC CLIP 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 1985-09-19 under 510(k) number K853650. 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 TITANIUM HEMOSTATIC CLIP?

AUTO SUTURE TITANIUM HEMOSTATIC CLIP is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K853650.

When did AUTO SUTURE TITANIUM HEMOSTATIC CLIP receive FDA 510(k) clearance?

AUTO SUTURE TITANIUM HEMOSTATIC CLIP received FDA 510(k) clearance on 1985-09-19, under 510(k) number K853650.

Who is the listed applicant for AUTO SUTURE TITANIUM HEMOSTATIC CLIP?

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 TITANIUM HEMOSTATIC CLIP?

The FDA product code for AUTO SUTURE TITANIUM HEMOSTATIC CLIP is FZP.

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Related Devices (Code: FZP)

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.

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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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