Siemens Medical Systems, Inc.
Siemens Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2014.
Top product codes for Siemens Medical Systems, Inc.
Recent clearances by Siemens Medical Systems, Inc.
- K133646 — ADMIRE
- K130901 — SOMATOM DEFINITION AS OPEN
- K123540 — SYNGO CT PULMO 3D
- K123541 — SYNGO.CT NEURO PERFUSION
- K122909 — SYNGO SINGLE SOURCE DUAL ENGERY
- K122471 — SOMATOM DEFINITION
- K120579 — SOMATOM DEFINITION EDGE
- K121072 — SOMATOM DEFINITION FLASH
- K113342 — SOMATOM DEFINITION FLASH
- K052216 — SOMATOM DEFINITION
- K051602 — AXIOM SIRESKOP SD
- K042646 — DYNACT
- K042328 — SOMATOM SPIRIT
- K040970 — LEONARDO
- K040675 — AXIOM ARTIS U
- K040577 — SOMATOM PROJECT P30L
- K040347 — SIREMOBIL ISO-C 3D
- K033238 — MOBILETTE XP AND MOBILETT XPHYBRID
- K020440 — NEWCOR
- K023687 — SOMATOM EMOTION 6 CT SYSTEMS
- K023571 — 6 CHANNEL BODY COIL
- K020353 — OMNIA X/XS ULTRASOUND SYSTEM
- K013826 — AXIOM ARISTOS FX (MULTI PURPOSE RADIOGRAPHY SYSTEM)
- K013586 — MAGNETOM TRIO SYSTEM
- K013522 — SOMATOM P30 CT SYSTEMS
Data sourced from openFDA. This site is unofficial and independent of the FDA.