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

CARDIOCAP MONITOR

K Number: K853953 · Decision Jun 2, 1986
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
20
Review Days
250

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Basic Information

Device Name
CARDIOCAP MONITOR
K Number
K853953
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Instrumentarium Corp.
Date Received
September 25, 1985
Decision Date
June 2, 1986
Product Code
DRT
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
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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