Boehringer Laboratories - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
FDA 510(k) cleared devices by Boehringer Laboratories General Hospital ✕
9 devices
Cleared
May 15, 2002
BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES
General Hospital
85d
Cleared
Jan 08, 2002
BOEHRINGER MRI SUCTION REGULATORY
General Hospital
36d
Cleared
Mar 28, 1994
BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED
General Hospital
265d
Cleared
Mar 03, 1989
REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES
General Hospital
155d
Cleared
Apr 28, 1986
T-VAC PLEURAL DRAINAGE UNIT, 7800 SERIES
General Hospital
41d
Cleared
Mar 13, 1986
FILTERED VACUUM SAFETY TRAP BOTTLE
General Hospital
84d
Cleared
Oct 16, 1985
BOEHRINGER LAB SUCTION INTERRUPTER
General Hospital
79d
Cleared
Aug 23, 1985
BOEHRINGER LABORATORIES SUCTION INTERMITTOR
General Hospital
31d
Cleared
Mar 04, 1985
SUCTION REGULATOR 7700 SERIES
General Hospital
45d