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FDA 510(k)

THE SAMUELS RETROGRAD VALVULOTOME

K-Number: K932009 · 1993-09-21

ApplicantVascutech, Inc.
Decision Date1993-09-21
Product CodeMGZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE SAMUELS RETROGRAD VALVULOTOME is the device name listed in this FDA 510(k) record. The listed applicant is Vascutech, Inc.. It received FDA 510(k) clearance on 1993-09-21 under 510(k) number K932009. The device is classified under product code MGZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SAMUELS RETROGRAD VALVULOTOME?

THE SAMUELS RETROGRAD VALVULOTOME is a medical device that received FDA 510(k) clearance on 1993-09-21. The listed applicant is Vascutech, Inc.. The 510(k) number is K932009.

When did THE SAMUELS RETROGRAD VALVULOTOME receive FDA 510(k) clearance?

THE SAMUELS RETROGRAD VALVULOTOME received FDA 510(k) clearance on 1993-09-21, under 510(k) number K932009.

Who is the listed applicant for THE SAMUELS RETROGRAD VALVULOTOME?

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

What is the FDA product code for THE SAMUELS RETROGRAD VALVULOTOME?

The FDA product code for THE SAMUELS RETROGRAD VALVULOTOME is MGZ.

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Other records listing Vascutech, Inc. as applicant

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K001621DARDIK CAROTID SHUNTK992942LEMAITRE OCCLUSION CATHETERK992933LEMAITRE IRRIGATION CATHETERK992934LEMAITRE VENOUS THROMBECTOMY CATHETERK992940LEMAITRE BALLOON CATHETER WITH IRRIGATIONK992941LEMAITRE BILIARY CATHETER

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Related Devices (Code: MGZ)

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.

K260188LimFlow VectorLimFlow, Inc.K250105Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125)Aveera Medical, Inc.K221902LimFlow VectorLimFlow, Inc.K190267EZE SIT ValvulotomeLemaitre VascularK132047LEMILLS VALVULOTOMELeMaitre Vascular, Inc.K132190EXPANDABLE LEMAITRE VALVULOTOME, OVER-THE-WIRE LEMAITRE VALVULOTOMELeMaitre Vascular, 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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