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

ELECATH(R) TRANSESOPHAGEAL PACING CATHETER

K Number: K874154 · Decision Apr 29, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
35
Review Days
199

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Basic Information

Device Name
ELECATH(R) TRANSESOPHAGEAL PACING CATHETER
K Number
K874154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
October 13, 1987
Decision Date
April 29, 1988
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

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
K854511 ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SET
K854975 ELECATH PULSATILE PERFUSION PUMP
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. →