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

ACCUNET EMBOLIC PROTECTION SYSTEM, RX ACCUNET EMBOLIC PROTECTION SYSTEM

K Number: K042218 · Decision Aug 31, 2004
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
35
Applicant Total
71
Review Days
26

Basic Information

Device Name
ACCUNET EMBOLIC PROTECTION SYSTEM, RX ACCUNET EMBOLIC PROTECTION SYSTEM
K Number
K042218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GUIDANT CORP.
Date Received
August 5, 2004
Decision Date
August 31, 2004
Product Code
NTE
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
NTE Temporary Carotid Catheter For Embolic Capture

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K031459 RAPIDO CUT-AWAY CUTTER
K031398 IS-1 HEMOSTASIS VALVE, MODEL 6799
K030512 GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM
K030019 MODIFICATION TO HI-TORQUE WHISPER GUIDEWIRE
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