Instrumentarium Imaging, Inc.
Instrumentarium Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2000.
Top product codes for Instrumentarium Imaging, Inc.
Recent clearances by Instrumentarium Imaging, Inc.
- K002472 — DELTA 32 AND DELTA 32 TACT
- K001928 — SIGMA
- K000976 — DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)
- K001171 — DELTA 16 TACT
- K973642 — ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100
- K955411 — DELTA 16
- K925987 — INSTRUMENTARIUM MEGA4 HT
- K924921 — INSTRUMENTARIUM MEGA4 HT
- K923581 — INSTRUMENTARIUM MEGA4 HT
- K924472 — INSTRUMENTARIUM MEGA4 HT
- K923352 — INSTRUMENTARIUM MEGA4 HT
- K923022 — INSTRUMENTARIUM MEGA4 HT
- K920215 — INSTRUMENTARIUM MEGA4 HT
- K915552 — INSTRUMENTARIUM MEGA4
- K912180 — MODEL MGB-301 DIAPHRAGM FILM 24 X 30 CM
- K912963 — INSTRUMENTARIUM MEGA4
- K910111 — VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS
- K896596 — ALPHA III PLUS AND MODEL P2500F/101 W/OPTIONAL
- K904528 — INSTRUMENTARIUM MEGA4, MODIFICATION
- K902044 — MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM
- K900967 — MODIFIED ALPHA MC-9R C-ARM
- K901620 — MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI
- K896309 — MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC
- K891543 — MAGNAVIEW MOBILE MRI VERSION 110 FHM
Data sourced from openFDA. This site is unofficial and independent of the FDA.