The Devilbiss Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Devilbiss Co. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
The Devilbiss Co. has 12 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1977 to 1987.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Devilbiss Co.
12 devices
Cleared
Dec 23, 1987
DEVILBISS MODEL 8500D
Anesthesiology
79d
Cleared
Oct 15, 1987
VACU-AIDE
General & Plastic Surgery
136d
Cleared
Sep 04, 1987
ULTRA-NEB 99 ULTRASONIC NEBULIZER
Anesthesiology
50d
Cleared
Aug 03, 1987
DEVO/MC44 OXYGEN CONCENTRATOR
Anesthesiology
87d
Cleared
Dec 09, 1985
PULMO-AIDE MODEL 5610D
Anesthesiology
27d
Cleared
Jun 24, 1985
DEVO/MC29 OXYGEN CONCENTRATOR MC29D
Anesthesiology
34d
Cleared
Jun 05, 1985
ULTRA-NEB 100 ULTRASONIC NEBULIZER
Cardiovascular
44d
Cleared
Feb 17, 1983
DE VO/44 OXYGEN CONCENTRATOR #444
Anesthesiology
30d
Cleared
Jul 21, 1980
SURVEYOR I, RESPIRATORY COMPUTER SYSTEM
Anesthesiology
19d
Cleared
Dec 05, 1979
DEVO OXYGEN CONCENTRATOR, MODEL 955
Anesthesiology
9d
Cleared
Sep 27, 1978
PULMO-SONIC
Anesthesiology
93d
Cleared
Feb 07, 1977
DEVILBISS OXYGEN ENRICHER
Anesthesiology
14d