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

VASCU-GUARD

K Number: K942010 · Decision Jul 7, 1994
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
89
Applicant Total
26
Review Days
73

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Basic Information

Device Name
VASCU-GUARD
K Number
K942010
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3470
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Vascular, Inc.
Date Received
April 25, 1994
Decision Date
July 7, 1994
Product Code
DXZ
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
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXZ), ordered by most recent decision date.

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Other Clearances by Bio-Vascular, Inc.

K Number Device Name
K002233 BVI SLING
K992537 PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATED
K983602 CV PERI-GUARD AND VASCU-GUARD
K983581 OCU-GUARD AND OCU-GUARD SUPPLE
K983162 PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC
K981624 FLO-THRU
K982282 DURA-GUARD - DURAL REPAIR PATCH
K971726 CV PERI-GUARD - CARDIOVASCULAR PATCH
K973706 DURA-GUARD-DURAL REPAIR PATCH
K973552 OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP
Search all 26 clearances from Bio-Vascular, Inc. →