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FDA 510(k)

RT DESKTOP

K-Number: K982713 · 1998-11-02

ApplicantElekta Oncology Systems, Ltd.
Decision Date1998-11-02
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RT DESKTOP is the device name listed in this FDA 510(k) record. The listed applicant is Elekta Oncology Systems, Ltd.. It received FDA 510(k) clearance on 1998-11-02 under 510(k) number K982713. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RT DESKTOP?

RT DESKTOP is a medical device that received FDA 510(k) clearance on 1998-11-02. The listed applicant is Elekta Oncology Systems, Ltd.. The 510(k) number is K982713.

When did RT DESKTOP receive FDA 510(k) clearance?

RT DESKTOP received FDA 510(k) clearance on 1998-11-02, under 510(k) number K982713.

Who is the listed applicant for RT DESKTOP?

The FDA 510(k) record lists Elekta Oncology Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RT DESKTOP?

The FDA product code for RT DESKTOP is IYE.

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 Elekta Oncology Systems, Ltd. 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.

K032996ELEKTA SYNERGY SYSTEMK012289MODIFICATION TO: VIEWGT ELECTRONIC PORTAL IMAGING DEVICE (EPID)K981790IVIEW ELECTRONIC PORTAL IMAGING DEVICE (EPID) MODEL NUMBER IVEW

Related Devices (Code: IYE)

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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