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FDA 510(k)

CET PROSTATE APPLICATOR SET, PART NUMBER 089.066

K-Number: K990990 · 1999-10-07

Decision Date1999-10-07
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CET PROSTATE APPLICATOR SET, PART NUMBER 089.066 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 1999-10-07 under 510(k) number K990990. 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 CET PROSTATE APPLICATOR SET, PART NUMBER 089.066?

CET PROSTATE APPLICATOR SET, PART NUMBER 089.066 is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Nucletron Corp.. The 510(k) number is K990990.

When did CET PROSTATE APPLICATOR SET, PART NUMBER 089.066 receive FDA 510(k) clearance?

CET PROSTATE APPLICATOR SET, PART NUMBER 089.066 received FDA 510(k) clearance on 1999-10-07, under 510(k) number K990990.

Who is the listed applicant for CET PROSTATE APPLICATOR SET, PART NUMBER 089.066?

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 CET PROSTATE APPLICATOR SET, PART NUMBER 089.066?

The FDA product code for CET PROSTATE APPLICATOR SET, PART NUMBER 089.066 is JAQ.

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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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