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

SPIROX A

K Number: K812959 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
9
Review Days
93

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Basic Information

Device Name
SPIROX A
K Number
K812959
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1850
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Cairco , Ltd.
Date Received
October 21, 1981
Decision Date
January 22, 1982
Product Code
BZK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BZK Spirometer, Monitoring (W/Wo Alarm)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BZK), ordered by most recent decision date.

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Other Clearances by Cairco , Ltd.

K Number Device Name
K812961 SHEFFIELD INFANT VENTILATOR MARK 4
K812957 EAST AUTOCLAVE HUMIDIFIER
K812956 SPIROX H
K812958 EAST-FREEMAN VENTILATOR MARK 2
K812955 EAST WATER UNIT MARK 3
K812953 RADCLIFFE VENTILATOR MARK 5
K812960 EAST VENTILARM PRESSURE MONITOR ALARM S.
K810640 POLARISED LIGHT GRONIOMETER