FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ELECATH PORTAL VEIN/BILIARY DRAIN ASSM

K Number: K821488 · Decision May 28, 1982
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
35
Review Days
10

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Basic Information

Device Name
ELECATH PORTAL VEIN/BILIARY DRAIN ASSM
K Number
K821488
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3920
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
May 18, 1982
Decision Date
May 28, 1982
Product Code
KNN
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
KNN Components, Wheelchair

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Other Clearances by Electro-Catheter Corp.

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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. →