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FDA 510(k)

MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS

K-Number: K853912 · 1986-05-21

ApplicantNucletron-Oldelft Corp.
Decision Date1986-05-21
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS 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 1986-05-21 under 510(k) number K853912. 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 MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS?

MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS is a medical device that received FDA 510(k) clearance on 1986-05-21. The listed applicant is Nucletron-Oldelft Corp.. The 510(k) number is K853912.

When did MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS receive FDA 510(k) clearance?

MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS received FDA 510(k) clearance on 1986-05-21, under 510(k) number K853912.

Who is the listed applicant for MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS?

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 MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS?

The FDA product code for MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS is JAQ.

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Related Devices (Code: JAQ)

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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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