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

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)

K Number: K902276 · Decision Aug 17, 1990
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
172
Review Days
88

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Basic Information

Device Name
RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)
K Number
K902276
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Respironics, Inc.
Date Received
May 21, 1990
Decision Date
August 17, 1990
Product Code
CAP
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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