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

PRESSURE ALARM

K Number: K782174 · Decision Jan 22, 1979
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
6
Review Days
34

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Basic Information

Device Name
PRESSURE ALARM
K Number
K782174
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Thompson Respiration Products, Inc.
Date Received
December 19, 1978
Decision Date
January 22, 1979
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)

Similar 510(k) Clearances

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

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Other Clearances by Thompson Respiration Products, Inc.

K Number Device Name
K822103 MODEL M3000XA VENTILATOR SPECIFICA
K781158 ALARM UNIT, BATTERY OPERATED
K781160 VENTILATOR, MINILUNG
K781159 VENTILATOR, PRESSURE
K781161 RESPIRATOR, BANTAM MODEL