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

GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000

K Number: K052274 · Decision Sep 21, 2005
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
30

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Basic Information

Device Name
GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000
K Number
K052274
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guidant Corporation
Date Received
August 22, 2005
Decision Date
September 21, 2005
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K Number Device Name
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K053019 ACUITY STEERABLE STYLET ACCESSORY
K052965 EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.
K052166 MODIFICATION TO: RX ACCUNET EMBOLIC PROTECTION SYSTEM
K052165 RX ACCUNET EMBOLIC PROTECTION SYSTEM
K041981 GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000; GUIDANT VASOVIEW 6 ACCESSORY PACK, MODEL VH-2004
K041762 FINISHING WIRE SUPPORTRAK
K041574 CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020
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