Medical Device Manufacturer · US , Tewksbury , MA

Instrumentarium Corp. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1983

Total

Cleared

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

1-12 of 20

Cleared Oct 09, 2002

MODIFICATION TO FOCUS

ORTHOPANTOMOGRAPH OP100D

K992385 · MUH

Radiology · 74d

Cleared Jul 17, 1998

MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST,...

K981641 · IZH

Radiology · 70d

Cleared Apr 04, 1997

TONOCAP, TC-200 AND ACCESSORY CATHETERS

K962638 · CCK

Anesthesiology · 273d

Cleared Apr 30, 1996

TONOMETERED SLAINE BLOOD GAS CONTROL

K961441 · JJS

Chemistry · 15d

Cleared Jan 30, 1996

TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR

K955018 · FFT

Gastroenterology & Urology · 89d

AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE

K923433 · CBQ

Anesthesiology · 374d

ORTHOPANTOMOGRAPH 100

K912893 · EHD

Radiology · 127d

Instrumentarium Corp. - FDA 510(k) Cleared Devices

Filters