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FDA 510(k)

SOMATOM P30 CT SYSTEMS

K-Number: K013522 · 2001-11-07

ApplicantSiemens Medical Systems, Inc.
Decision Date2001-11-07
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM P30 CT SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Systems, Inc.. It received FDA 510(k) clearance on 2001-11-07 under 510(k) number K013522. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOMATOM P30 CT SYSTEMS?

SOMATOM P30 CT SYSTEMS is a medical device that received FDA 510(k) clearance on 2001-11-07. The listed applicant is Siemens Medical Systems, Inc.. The 510(k) number is K013522.

When did SOMATOM P30 CT SYSTEMS receive FDA 510(k) clearance?

SOMATOM P30 CT SYSTEMS received FDA 510(k) clearance on 2001-11-07, under 510(k) number K013522.

Who is the listed applicant for SOMATOM P30 CT SYSTEMS?

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

What is the FDA product code for SOMATOM P30 CT SYSTEMS?

The FDA product code for SOMATOM P30 CT SYSTEMS is JAK.

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Other records listing Siemens Medical Systems, Inc. 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.

K123540SYNGO CT PULMO 3DK123541SYNGO.CT NEURO PERFUSIONK122909SYNGO SINGLE SOURCE DUAL ENGERYK122471SOMATOM DEFINITIONK120579SOMATOM DEFINITION EDGEK121072SOMATOM DEFINITION FLASH

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Related Devices (Code: JAK)

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.

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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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