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FDA 510(k)

CURIETRON

K-Number: K840127 · 1984-03-19

ApplicantSyncor Intl. Corp.
Decision Date1984-03-19
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CURIETRON is the device name listed in this FDA 510(k) record. The listed applicant is Syncor Intl. Corp.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840127. 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 CURIETRON?

CURIETRON is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Syncor Intl. Corp.. The 510(k) number is K840127.

When did CURIETRON receive FDA 510(k) clearance?

CURIETRON received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840127.

Who is the listed applicant for CURIETRON?

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

What is the FDA product code for CURIETRON?

The FDA product code for CURIETRON is JAQ.

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Other records listing Syncor Intl. Corp. as applicant

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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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