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FDA 510(k)

LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER

K-Number: K023688 · 2003-01-30

ApplicantLeMaitre Vascular, Inc.
Decision Date2003-01-30
Product CodeGAF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER is the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2003-01-30 under 510(k) number K023688. The device is classified under product code GAF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER?

LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER is a medical device that received FDA 510(k) clearance on 2003-01-30. The listed applicant is LeMaitre Vascular, Inc.. The 510(k) number is K023688.

When did LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER receive FDA 510(k) clearance?

LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER received FDA 510(k) clearance on 2003-01-30, under 510(k) number K023688.

Who is the listed applicant for LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER?

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

What is the FDA product code for LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER?

The FDA product code for LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER is GAF.

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Other records listing LeMaitre Vascular, Inc. 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.

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Related Devices (Code: GAF)

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.

K935357SNAP RECIPROCATING SAWSurgiquip, Inc.K890374ABDOMINAL SPATULAKinetic Medical ProductsK882793PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINEPmt Corp.K822108CEMENT-PICKBio-Blitz, Inc.

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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