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

VASOSTASIS VASCULAR CLOSURE SYSTEM

K Number: K041486 · Decision Oct 22, 2004
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
7
Review Days
140

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Basic Information

Device Name
VASOSTASIS VASCULAR CLOSURE SYSTEM
K Number
K041486
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiva Medical, Inc.
Date Received
June 4, 2004
Decision Date
October 22, 2004
Product Code
DXC
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
DXC Clamp, Vascular

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K Number Device Name
K130124 CATALYST II AND III
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K072297 BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM
K070485 BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L
K051817 BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM
K061075 BOOMERANG WIRE