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FDA 510(k)

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

K-Number: K760604 · 1976-09-13

ApplicantEureka X-Ray Tube Corp.
Decision Date1976-09-13
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS. 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 1976-09-13 under 510(k) number K760604. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS.?

EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS. is a medical device that received FDA 510(k) clearance on 1976-09-13. The listed applicant is Eureka X-Ray Tube Corp.. The 510(k) number is K760604.

When did EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS. receive FDA 510(k) clearance?

EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS. received FDA 510(k) clearance on 1976-09-13, under 510(k) number K760604.

Who is the listed applicant for EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS.?

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

The FDA product code for EUREKA X-SCAN 150 X-RAY TUBE HOUSING AS. is ITY.

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.

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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.

K904489EUREKA EXTENSION CYLINDERS

Related Devices (Code: ITY)

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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

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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