Instrumentarium Imaging, Inc.
FDA 510(k) medical device clearances.
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.