FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

CARDIOCAP II TM CH-RESP MONITORS

K Number: K904355 · Decision May 23, 1991
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
20
Review Days
241

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Basic Information

Device Name
CARDIOCAP II TM CH-RESP MONITORS
K Number
K904355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Instrumentarium Corp.
Date Received
September 24, 1990
Decision Date
May 23, 1991
Product Code
DPS
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
DPS Electrocardiograph

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