FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LEMAITRE-BOOKWALTER VESSEL DEVICES

K Number: K912548 · Decision Sep 18, 1991
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
19
Applicant Total
14
Review Days
100

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Basic Information

Device Name
LEMAITRE-BOOKWALTER VESSEL DEVICES
K Number
K912548
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4475
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vascutech, Inc.
Date Received
June 10, 1991
Decision Date
September 18, 1991
Product Code
DWP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWP Dilator, Vessel, Surgical

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Other Clearances by Vascutech, Inc.

K Number Device Name
K001621 DARDIK CAROTID SHUNT
K992942 LEMAITRE OCCLUSION CATHETER
K992933 LEMAITRE IRRIGATION CATHETER
K992934 LEMAITRE VENOUS THROMBECTOMY CATHETER
K992940 LEMAITRE BALLOON CATHETER WITH IRRIGATION
K992941 LEMAITRE BILIARY CATHETER
K992368 LEMAITRE EMBOLECTOMY CATHETER
K980723 2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT)
K946352 LEMAITRE VALVULOTOME II
K932009 THE SAMUELS RETROGRAD VALVULOTOME
Search all 14 clearances from Vascutech, Inc. →