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FDA 510(k)

NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2

K-Number: K964206 · 1997-06-20

ApplicantNucletron Corp.
Decision Date1997-06-20
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 1997-06-20 under 510(k) number K964206. 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 NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2?

NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2 is a medical device that received FDA 510(k) clearance on 1997-06-20. The listed applicant is Nucletron Corp.. The 510(k) number is K964206.

When did NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2 receive FDA 510(k) clearance?

NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2 received FDA 510(k) clearance on 1997-06-20, under 510(k) number K964206.

Who is the listed applicant for NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2?

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 NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2?

The FDA product code for NUCLETRON PLATO EXTERNAL BEAM PLANNING RTS V2 AND RTS 3D V2 is IYE.

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Other records listing Nucletron Corp. as applicant

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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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