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FDA 510(k)

TITANIUM HEMOSTATIC CLIP

K-Number: K981645 · 1998-10-13

ApplicantVitalitec Int'L., Inc.
Decision Date1998-10-13
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TITANIUM HEMOSTATIC CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Vitalitec Int'L., Inc.. It received FDA 510(k) clearance on 1998-10-13 under 510(k) number K981645. 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 TITANIUM HEMOSTATIC CLIP?

TITANIUM HEMOSTATIC CLIP is a medical device that received FDA 510(k) clearance on 1998-10-13. The listed applicant is Vitalitec Int'L., Inc.. The 510(k) number is K981645.

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

TITANIUM HEMOSTATIC CLIP received FDA 510(k) clearance on 1998-10-13, under 510(k) number K981645.

Who is the listed applicant for TITANIUM HEMOSTATIC CLIP?

The FDA 510(k) record lists Vitalitec Int'L., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM HEMOSTATIC CLIP?

The FDA product code for TITANIUM HEMOSTATIC CLIP is FZP.

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Related Devices (Code: FZP)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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