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

ELECATH PULSATILE PERFUSION PUMP

K Number: K854975 · Decision Jan 15, 1986
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
83
Applicant Total
35
Review Days
34

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Basic Information

Device Name
ELECATH PULSATILE PERFUSION PUMP
K Number
K854975
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
December 12, 1985
Decision Date
January 15, 1986
Product Code
KFM
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
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

Similar 510(k) Clearances

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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
K850065 ELECATH TORKFLOAT PACING PROBE
K850324 ELECATH OPEN TIP BIPOLAR PACING CATHETER
K844682 ELECATH CARDIAC OUTPUT COMPUTER
Search all 35 clearances from Electro-Catheter Corp. →