PLATO BRACHYTHERAPHY, MODEL V. 14.0
K-Number: K983343 · 1999-04-02
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Device Summary
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.
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
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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