Boehringer Laboratories - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
FDA 510(k) cleared devices by Boehringer Laboratories Anesthesiology ✕
21 devices
Cleared
Feb 06, 2002
AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM
Anesthesiology
47d
Cleared
Jun 20, 1996
AUTOVAC BP SYSTE, 2000 SERIES
Anesthesiology
232d
Cleared
Oct 19, 1995
BOEHRINGER AUTOVAC(R) 7900 SERIES
Anesthesiology
328d
Cleared
Jul 06, 1994
AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S
Anesthesiology
432d
Cleared
Feb 05, 1993
AUTOVAC 7900 SERIES
Anesthesiology
130d
Cleared
Sep 06, 1991
AUTOVAC (R) AUTOTRANSFUSION SYSTEM, 7900 MODIFIED
Anesthesiology
360d
Cleared
Jan 16, 1991
AUTOWAND(TM) 7XXX SERIES, MODIFICATION
Anesthesiology
82d
Cleared
Jul 24, 1990
AUTOWAND(TM) 7XXX SERIES
Anesthesiology
78d
Cleared
Jun 18, 1990
AUTOVAC(R) AUTOTRANSFUSION SYSTEM, 7900 SERIES
Anesthesiology
98d
Cleared
Mar 13, 1990
AUTOTRANSFUSION RESERVIOR MODEL 7900 MODIFICATION
Anesthesiology
200d
Cleared
Jun 14, 1988
AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904
Anesthesiology
90d
Cleared
Mar 02, 1988
BRONCHODILATOR TEE - 9056 SERIES
Anesthesiology
183d