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FDA 510(k)

ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM

K-Number: K993923 · 2000-04-07

ApplicantAdac Laboratories
Decision Date2000-04-07
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADAC PINNACLE3TM RADIATION THERAPY PLANNING 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 2000-04-07 under 510(k) number K993923. 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 ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM?

ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM is a medical device that received FDA 510(k) clearance on 2000-04-07. The listed applicant is Adac Laboratories. The 510(k) number is K993923.

When did ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM receive FDA 510(k) clearance?

ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM received FDA 510(k) clearance on 2000-04-07, under 510(k) number K993923.

Who is the listed applicant for ADAC PINNACLE3TM RADIATION THERAPY PLANNING 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 ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM?

The FDA product code for ADAC PINNACLE3TM RADIATION THERAPY PLANNING SYSTEM is MUJ.

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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: 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.

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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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