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FDA 510(k)

CURIETRON 192 HIGH DOSE RATE

K-Number: K890799 · 1989-10-27

ApplicantCis-Us, Inc.
Decision Date1989-10-27
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CURIETRON 192 HIGH DOSE RATE is the device name listed in this FDA 510(k) record. The listed applicant is Cis-Us, Inc.. It received FDA 510(k) clearance on 1989-10-27 under 510(k) number K890799. 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 192 HIGH DOSE RATE?

CURIETRON 192 HIGH DOSE RATE is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Cis-Us, Inc.. The 510(k) number is K890799.

When did CURIETRON 192 HIGH DOSE RATE receive FDA 510(k) clearance?

CURIETRON 192 HIGH DOSE RATE received FDA 510(k) clearance on 1989-10-27, under 510(k) number K890799.

Who is the listed applicant for CURIETRON 192 HIGH DOSE RATE?

The FDA 510(k) record lists Cis-Us, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURIETRON 192 HIGH DOSE RATE?

The FDA product code for CURIETRON 192 HIGH DOSE RATE is JAQ.

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Other records listing Cis-Us, Inc. 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)

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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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