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FDA 510(k)

WEXLER VASCULAR CLAMP SERIES

K-Number: K110148 · 2011-04-19

Decision Date2011-04-19
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WEXLER VASCULAR CLAMP SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Microsurgical Laboratories,Inc.Dba Wexler Surgical. It received FDA 510(k) clearance on 2011-04-19 under 510(k) number K110148. 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 WEXLER VASCULAR CLAMP SERIES?

WEXLER VASCULAR CLAMP SERIES is a medical device that received FDA 510(k) clearance on 2011-04-19. The listed applicant is Microsurgical Laboratories,Inc.Dba Wexler Surgical. The 510(k) number is K110148.

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

WEXLER VASCULAR CLAMP SERIES received FDA 510(k) clearance on 2011-04-19, under 510(k) number K110148.

Who is the listed applicant for WEXLER VASCULAR CLAMP SERIES?

The FDA 510(k) record lists Microsurgical Laboratories,Inc.Dba Wexler Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEXLER VASCULAR CLAMP SERIES?

The FDA product code for WEXLER VASCULAR CLAMP SERIES is DXC.

Related Clinical Trials

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.

Other records listing Microsurgical Laboratories,Inc.Dba Wexler Surgical as applicant

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.

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.

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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