Instrumentarium Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Instrumentarium Corp. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Instrumentarium Corp. has 20 FDA 510(k) cleared medical devices. Based in Tewksbury, US.
Historical record: 20 cleared submissions from 1983 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Instrumentarium Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Instrumentarium Corp.
20 devices
Cleared
Oct 09, 2002
MODIFICATION TO FOCUS
Radiology
63d
Cleared
Jul 13, 2000
FOCUS
Radiology
36d
Cleared
Jun 22, 2000
ORTHOCEPH OC100 D
Radiology
45d
Cleared
Sep 28, 1999
ORTHOPANTOMOGRAPH OP100D
Radiology
74d
Cleared
Jul 17, 1998
MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST,...
Radiology
70d
Cleared
Apr 04, 1997
TONOCAP, TC-200 AND ACCESSORY CATHETERS
Anesthesiology
273d
Cleared
Apr 30, 1996
TONOMETERED SLAINE BLOOD GAS CONTROL
Chemistry
15d
Cleared
Jan 30, 1996
TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR
Gastroenterology & Urology
89d
Cleared
Jan 31, 1995
ALPHA STEREO
Radiology
504d
Cleared
Jul 22, 1993
AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE
Anesthesiology
374d
Cleared
Apr 27, 1993
ORTHOCEPH OC100
Radiology
92d
Cleared
Nov 05, 1991
ORTHOPANTOMOGRAPH 100
Radiology
127d