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FDA 510(k)

EUREKA EXTENSION CYLINDERS

K-Number: K904489 · 1990-10-15

ApplicantEureka X-Ray Tube Corp.
Decision Date1990-10-15
Product CodeKPW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EUREKA EXTENSION CYLINDERS is the device name listed in this FDA 510(k) record. The listed applicant is Eureka X-Ray Tube Corp.. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K904489. The device is classified under product code KPW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUREKA EXTENSION CYLINDERS?

EUREKA EXTENSION CYLINDERS is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Eureka X-Ray Tube Corp.. The 510(k) number is K904489.

When did EUREKA EXTENSION CYLINDERS receive FDA 510(k) clearance?

EUREKA EXTENSION CYLINDERS received FDA 510(k) clearance on 1990-10-15, under 510(k) number K904489.

Who is the listed applicant for EUREKA EXTENSION CYLINDERS?

The FDA 510(k) record lists Eureka X-Ray Tube Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUREKA EXTENSION CYLINDERS?

The FDA product code for EUREKA EXTENSION CYLINDERS is KPW.

Related Clinical Trials

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Other records listing Eureka X-Ray Tube 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.

K760604EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS.

Related Devices (Code: KPW)

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.

K093596LUMOS, MODEL R 72BLumos, Inc.K062788COLLIMATOR, MODEL M-38Umi InternationalK030487R 72Ralco S.R.L.K954310BLA-800AToshiba Medical SystemsK946320R 302Ralco S.R.L.K914184P2020-8-0 BEAM-LIMITING DEVICEPrecise Optics

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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