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

LEMAITRE BALLOON CATHETER WITH IRRIGATION

K Number: K992940 · Decision Feb 22, 2000
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
14
Review Days
175

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Basic Information

Device Name
LEMAITRE BALLOON CATHETER WITH IRRIGATION
K Number
K992940
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vascutech, Inc.
Date Received
August 31, 1999
Decision Date
February 22, 2000
Product Code
DXE
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
DXE Catheter, Embolectomy

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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
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
K932184 STERILE LEMAITRE GLOW 'N TELL TAPE
Search all 14 clearances from Vascutech, Inc. →