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

NOVA ARTERIAL EMBOLECTOMY CATHETER

K Number: K853625 · Decision Jan 15, 1986
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
11
Review Days
139

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Basic Information

Device Name
NOVA ARTERIAL EMBOLECTOMY CATHETER
K Number
K853625
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Nova Medical Specialties
Date Received
August 29, 1985
Decision Date
January 15, 1986
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 Nova Medical Specialties

K Number Device Name
K872770 DUAL-THERMISTOR THERMODILUTION CATH. & INFU. CATH.
K860526 NOVA BALLOON THERMODILUTION PRESSURE TRANS CATH
K840009 NOVA 12 CARDIAC OUTPUT COMPUTER
K841639 NOVA BALLOON THERMODILUTION CATH.
K841640 NOVA BALLOON THERMODILUTION INFUSION
K834036 HEPARIN COATED BALLOON THERMODILU
K834037 HEPARIN COATED BALLOON THERMODILU
K832287 NOVA BALLOON THERMODILUTION INFUSION
K822806 BALLOON WEDGE PRESSURE, ANGIOGRAPHIC
K812761 FLOW-DIRECTED BALLOON THERMODILUTION
Search all 11 clearances from Nova Medical Specialties →