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FDA 510(k)

Multitom Rax with True2scale Body Scan Option

K-Number: K212212 · 2022-02-18

ApplicantSiemens Medical Solutions
Decision Date2022-02-18
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Multitom Rax with True2scale Body Scan Option is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions. It received FDA 510(k) clearance on 2022-02-18 under 510(k) number K212212. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Multitom Rax with True2scale Body Scan Option?

Multitom Rax with True2scale Body Scan Option is a medical device that received FDA 510(k) clearance on 2022-02-18. The listed applicant is Siemens Medical Solutions. The 510(k) number is K212212.

When did Multitom Rax with True2scale Body Scan Option receive FDA 510(k) clearance?

Multitom Rax with True2scale Body Scan Option received FDA 510(k) clearance on 2022-02-18, under 510(k) number K212212.

Who is the listed applicant for Multitom Rax with True2scale Body Scan Option?

The FDA 510(k) record lists Siemens Medical Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multitom Rax with True2scale Body Scan Option?

The FDA product code for Multitom Rax with True2scale Body Scan Option is OWB.

Other records listing Siemens Medical Solutions as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250738YSIO X.preeK250660LUMINOS Q.namix T; LUMINOS Q.namix RK233543YSIO X.preeK233532MULTIX Impact EK231577MOBILETT ImpactK221281Multitom Rax

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Related Devices (Code: OWB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254205Zenition 30Philips Medical Systems Nederland B.V.K260607Shield System (Siemens 30x40)Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.K252503Intelligent NRCanon, Inc.K254173ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS phenoSiemens Medical Solutions USA, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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