Thompson Respiration Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Thompson Respiration Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1982. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Thompson Respiration Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thompson Respiration Products, Inc.
6 devices
Cleared
Jul 26, 1982
MODEL M3000XA VENTILATOR SPECIFICA
Anesthesiology
10d
Cleared
Jan 22, 1979
PRESSURE ALARM
Anesthesiology
34d
Cleared
Dec 18, 1978
ALARM UNIT, BATTERY OPERATED
Anesthesiology
166d
Cleared
Dec 13, 1978
VENTILATOR, MINILUNG
Anesthesiology
161d
Cleared
Dec 12, 1978
VENTILATOR, PRESSURE
Anesthesiology
160d
Cleared
Dec 11, 1978
RESPIRATOR, BANTAM MODEL
Anesthesiology
159d