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FDA 510(k)

SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE

K-Number: K042229 · 2004-09-01

Decision Date2004-09-01
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solution, Inc. USA. It received FDA 510(k) clearance on 2004-09-01 under 510(k) number K042229. 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 RADIATION TREATMENT PLANNING (RTP) PACKAGE?

SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE is a medical device that received FDA 510(k) clearance on 2004-09-01. The listed applicant is Siemens Medical Solution, Inc. USA. The 510(k) number is K042229.

When did SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE receive FDA 510(k) clearance?

SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE received FDA 510(k) clearance on 2004-09-01, under 510(k) number K042229.

Who is the listed applicant for SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE?

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

What is the FDA product code for SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE?

The FDA product code for SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE is JAK.

Related Clinical Trials

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.

Other records listing Siemens Medical Solution, Inc. USA 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.

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.

Official Source

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

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