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FDA 510(k)

VASCULAR CLAMP

K-Number: K895691 · 1989-12-13

ApplicantApplied Vascular Devices, Inc.
Decision Date1989-12-13
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAR CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Applied Vascular Devices, Inc.. It received FDA 510(k) clearance on 1989-12-13 under 510(k) number K895691. 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 VASCULAR CLAMP?

VASCULAR CLAMP is a medical device that received FDA 510(k) clearance on 1989-12-13. The listed applicant is Applied Vascular Devices, Inc.. The 510(k) number is K895691.

When did VASCULAR CLAMP receive FDA 510(k) clearance?

VASCULAR CLAMP received FDA 510(k) clearance on 1989-12-13, under 510(k) number K895691.

Who is the listed applicant for VASCULAR CLAMP?

The FDA 510(k) record lists Applied Vascular Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR CLAMP?

The FDA product code for VASCULAR CLAMP is DXC.

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Other records listing Applied Vascular Devices, Inc. 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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