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FDA 510(k)

RADIATION ONCOLOGY SYSTEM

K-Number: K782005 · 1978-12-20

ApplicantAdac Laboratories
Decision Date1978-12-20
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIATION ONCOLOGY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K782005. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIATION ONCOLOGY SYSTEM?

RADIATION ONCOLOGY SYSTEM is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Adac Laboratories. The 510(k) number is K782005.

When did RADIATION ONCOLOGY SYSTEM receive FDA 510(k) clearance?

RADIATION ONCOLOGY SYSTEM received FDA 510(k) clearance on 1978-12-20, under 510(k) number K782005.

Who is the listed applicant for RADIATION ONCOLOGY SYSTEM?

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

What is the FDA product code for RADIATION ONCOLOGY SYSTEM?

The FDA product code for RADIATION ONCOLOGY SYSTEM is KPQ.

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Other records listing Adac Laboratories 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.

K062298APOLLO GAMMA CAMERA SYSTEMK061029JETSTREAM WORKSPACEK060020AUTOQUANT PLUSK051351PRECEDENCE SPECT/CT IMAGING SYSTEMK042880JETSTREAM WORKSPACEK042903AUTOSPECS

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Related Devices (Code: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, LLC

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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