Instrumentarium Corp.
FDA 510(k) medical device clearances.
Top product codes for Instrumentarium Corp.
Recent clearances by Instrumentarium Corp.
- K022630 — MODIFICATION TO FOCUS
- K001729 — FOCUS
- K001439 — ORTHOCEPH OC100 D
- K992385 — ORTHOPANTOMOGRAPH OP100D
- K981641 — MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQ
- K962638 — TONOCAP, TC-200 AND ACCESSORY CATHETERS
- K961441 — TONOMETERED SLAINE BLOOD GAS CONTROL
- K955018 — TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR
- K934478 — ALPHA STEREO
- K923433 — AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE
- K930338 — ORTHOCEPH OC100
- K912893 — ORTHOPANTOMOGRAPH 100
- K904355 — CARDIOCAP II TM CH-RESP MONITORS
- K883621 — INSTRUMENTARIUM ULF MR IMAGING SYSTEM
- K883649 — INSTRUMENTARIUM ULF MR IMAGING SYSTEM MODEL 110H
- K883650 — INSTRUMENTARIUM ULF MR IMAGING SYSTEM VERSION 110
- K883622 — INSTRUMENTARIUM ULF MR IMAGING SYSTEM
- K853953 — CARDIOCAP MONITOR
- K853396 — MULTICAP MULTIGAS CAPNOMETER PB252
- K833739 — CD-102 CARBON DIOXIDE ANALYZER/RECOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.