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

DIGITAL BPM

K Number: K790036 · Decision Mar 2, 1979
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
19
Review Days
53

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Basic Information

Device Name
DIGITAL BPM
K Number
K790036
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Narco Air-Shields
Date Received
January 8, 1979
Decision Date
March 2, 1979
Product Code
DXO
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
DXO Transducer, Pressure, Catheter Tip

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K Number Device Name
K820114 SYSTEM V.HEART RATE/RESPIR. RATE MONIT.
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K802800 NARCO AIR-SHEILDS SYS. 100 MONITOR SYS
K802126 ISOLETTE INCUBATOR C-100
K792592 AMBU UNIVERSAL SUCTION PUMP
K792499 AMBU PAEDI ANAESTHESIA SYSTEM
K792117 AIR-SHIELDS HEART RATE MONITOR
K792118 AIR-SHIELDS RESUSCITATORS
K790552 AS7 & AS8 MONITORS
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