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

ELECATH INFANT ARTERIAL & VENOUS CANNU

K Number: K842369 · Decision Aug 27, 1984
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
35
Review Days
73

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Basic Information

Device Name
ELECATH INFANT ARTERIAL & VENOUS CANNU
K Number
K842369
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
June 15, 1984
Decision Date
August 27, 1984
Product Code
BWF
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BWF Spirometer, Therapeutic (Incentive)

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
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. →