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FDA 510(k)

FLEXIBLE VASCULAR CLAMP, VERSION 2

K-Number: K991589 · 1999-05-18

ApplicantAllegiance Healthcare Corp.
Decision Date1999-05-18
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE VASCULAR CLAMP, VERSION 2 is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 1999-05-18 under 510(k) number K991589. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE VASCULAR CLAMP, VERSION 2?

FLEXIBLE VASCULAR CLAMP, VERSION 2 is a medical device that received FDA 510(k) clearance on 1999-05-18. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K991589.

When did FLEXIBLE VASCULAR CLAMP, VERSION 2 receive FDA 510(k) clearance?

FLEXIBLE VASCULAR CLAMP, VERSION 2 received FDA 510(k) clearance on 1999-05-18, under 510(k) number K991589.

Who is the listed applicant for FLEXIBLE VASCULAR CLAMP, VERSION 2?

The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEXIBLE VASCULAR CLAMP, VERSION 2?

The FDA product code for FLEXIBLE VASCULAR CLAMP, VERSION 2 is DXC.

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Other records listing Allegiance Healthcare Corp. as applicant

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Related Devices (Code: DXC)

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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