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

CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410

K Number: K043454 · Decision Mar 24, 2005
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
31
Applicant Total
23
Review Days
99

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Basic Information

Device Name
CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410
K Number
K043454
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicomp, Inc.
Date Received
December 15, 2004
Decision Date
March 24, 2005
Product Code
MLO
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
MLO Electrocardiograph, Ambulatory, With Analysis Algorithm

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Other Clearances by Medicomp, Inc.

K Number Device Name
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K090834 EPICARDIA 5000
K981119 CARDIOPAL MODEL NUMBER PM20
K952846 EPICARDIA
K943915 HEAT AND MOISTURE EXCHANGER FILTER (HME)
K900207 EPICARDIA 4000
K883103 EPICARDIA PC/FC
K881770 EPICARDIA LE/FD
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