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

EPICARDIA 4000

K Number: K900207 · Decision Jul 31, 1990
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
23
Review Days
196

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Basic Information

Device Name
EPICARDIA 4000
K Number
K900207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Medicomp, Inc.
Date Received
January 16, 1990
Decision Date
July 31, 1990
Product Code
DST
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
DST Clip, Vena-Cava

Other Clearances by Medicomp, Inc.

K Number Device Name
K173170 Epicardia Anywhere
K161916 TelePatch Cardiac Monitor
K091696 SAVI WIRELESS, MODEL PM500
K090834 EPICARDIA 5000
K043454 CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410
K981119 CARDIOPAL MODEL NUMBER PM20
K952846 EPICARDIA
K943915 HEAT AND MOISTURE EXCHANGER FILTER (HME)
K883103 EPICARDIA PC/FC
K881770 EPICARDIA LE/FD
Search all 23 clearances from Medicomp, Inc. →