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

ELECATH ARTERIAL EMBOLECTOMY CATHETER

K Number: K761031 · Decision Dec 13, 1976
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
35
Review Days
28

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Basic Information

Device Name
ELECATH ARTERIAL EMBOLECTOMY CATHETER
K Number
K761031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
November 15, 1976
Decision Date
December 13, 1976
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 Electro-Catheter Corp.

K Number Device Name
K934785 MULTIPACE
K933450 CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATION
K943257 TIP DEFLECTOR (GENESIS)
K933451 OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATION
K934787 SILICORE SEMI-FLOATER
K874154 ELECATH(R) TRANSESOPHAGEAL PACING CATHETER
K854511 ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SET
K854975 ELECATH PULSATILE PERFUSION PUMP
K850065 ELECATH TORKFLOAT PACING PROBE
K850324 ELECATH OPEN TIP BIPOLAR PACING CATHETER
Search all 35 clearances from Electro-Catheter Corp. →