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FDA 510(k)

HOFMANN-NAGEL (HOFNA) X-RAY TUBES

K-Number: K900367 · 1990-02-26

ApplicantHofmann
Decision Date1990-02-26
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HOFMANN-NAGEL (HOFNA) X-RAY TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Hofmann. It received FDA 510(k) clearance on 1990-02-26 under 510(k) number K900367. 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 HOFMANN-NAGEL (HOFNA) X-RAY TUBES?

HOFMANN-NAGEL (HOFNA) X-RAY TUBES is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Hofmann. The 510(k) number is K900367.

When did HOFMANN-NAGEL (HOFNA) X-RAY TUBES receive FDA 510(k) clearance?

HOFMANN-NAGEL (HOFNA) X-RAY TUBES received FDA 510(k) clearance on 1990-02-26, under 510(k) number K900367.

Who is the listed applicant for HOFMANN-NAGEL (HOFNA) X-RAY TUBES?

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

What is the FDA product code for HOFMANN-NAGEL (HOFNA) X-RAY TUBES?

The FDA product code for HOFMANN-NAGEL (HOFNA) X-RAY TUBES is ITY.

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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

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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