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FDA 510(k)

PLATO BRACHYTHERAPHY, MODEL V. 14.0

K-Number: K983343 · 1999-04-02

Decision Date1999-04-02
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PLATO BRACHYTHERAPHY, MODEL V. 14.0 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 1999-04-02 under 510(k) number K983343. 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 PLATO BRACHYTHERAPHY, MODEL V. 14.0?

PLATO BRACHYTHERAPHY, MODEL V. 14.0 is a medical device that received FDA 510(k) clearance on 1999-04-02. The listed applicant is Nucletron Corp.. The 510(k) number is K983343.

When did PLATO BRACHYTHERAPHY, MODEL V. 14.0 receive FDA 510(k) clearance?

PLATO BRACHYTHERAPHY, MODEL V. 14.0 received FDA 510(k) clearance on 1999-04-02, under 510(k) number K983343.

Who is the listed applicant for PLATO BRACHYTHERAPHY, MODEL V. 14.0?

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

What is the FDA product code for PLATO BRACHYTHERAPHY, MODEL V. 14.0?

The FDA product code for PLATO BRACHYTHERAPHY, MODEL V. 14.0 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.

Other records listing Nucletron Corp. 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.

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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.

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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