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FDA 510(k)

SELECTRON HDR REMOTE AFTERLOADER

K-Number: K852842 · 1986-01-10

ApplicantNucletron-Oldelft Corp.
Decision Date1986-01-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SELECTRON HDR REMOTE AFTERLOADER is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron-Oldelft Corp.. It received FDA 510(k) clearance on 1986-01-10 under 510(k) number K852842. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELECTRON HDR REMOTE AFTERLOADER?

SELECTRON HDR REMOTE AFTERLOADER is a medical device that received FDA 510(k) clearance on 1986-01-10. The listed applicant is Nucletron-Oldelft Corp.. The 510(k) number is K852842.

When did SELECTRON HDR REMOTE AFTERLOADER receive FDA 510(k) clearance?

SELECTRON HDR REMOTE AFTERLOADER received FDA 510(k) clearance on 1986-01-10, under 510(k) number K852842.

Who is the listed applicant for SELECTRON HDR REMOTE AFTERLOADER?

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

What is the FDA product code for SELECTRON HDR REMOTE AFTERLOADER?

The FDA product code for SELECTRON HDR REMOTE AFTERLOADER is JAQ.

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Other records listing Nucletron-Oldelft Corp. as applicant

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Related Devices (Code: JAQ)

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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