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FDA 510(k)

FOCUS RTP

K-Number: K915691 · 1995-02-16

ApplicantComputerized Medical Systems, Inc.
Decision Date1995-02-16
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FOCUS RTP is the device name listed in this FDA 510(k) record. The listed applicant is Computerized Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-02-16 under 510(k) number K915691. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOCUS RTP?

FOCUS RTP is a medical device that received FDA 510(k) clearance on 1995-02-16. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K915691.

When did FOCUS RTP receive FDA 510(k) clearance?

FOCUS RTP received FDA 510(k) clearance on 1995-02-16, under 510(k) number K915691.

Who is the listed applicant for FOCUS RTP?

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

What is the FDA product code for FOCUS RTP?

The FDA product code for FOCUS RTP is MUJ.

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.

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Other records listing Computerized 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.

K110730MONACO RTP SYSTEMK102216XIO RTP SYSTEMK092132XIO RTP SYSTEMK091179MONACO RTP SYSTEM, VMAT OPTIONK080799ATLAS-BASED AUTOSEGMENTATIONK071938MONACO RTP SYSTEM

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Related Devices (Code: MUJ)

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.

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformaiK260207Multimodality Simulation Workspace (MM Sim) (v1.0.0)Philips Medical Systems Nederland B.V.K252784eXaSkin PlusAnatomical Geometry S.L.K253078ART.1-USSeetreat Pty, Ltd.K252304syngo.via RT Image Suite VC10Varian Medical Systems, 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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