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FDA 510(k)

DIAGNOSTIC X-RAY HV GENERATOR

K-Number: K827378 · 1982-05-19

ApplicantTechnicare Corp.
Decision Date1982-05-19
Product Code
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC X-RAY HV GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1982-05-19 under 510(k) number K827378. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC X-RAY HV GENERATOR?

DIAGNOSTIC X-RAY HV GENERATOR is a medical device that received FDA 510(k) clearance on 1982-05-19. The listed applicant is Technicare Corp.. The 510(k) number is K827378.

When did DIAGNOSTIC X-RAY HV GENERATOR receive FDA 510(k) clearance?

DIAGNOSTIC X-RAY HV GENERATOR received FDA 510(k) clearance on 1982-05-19, under 510(k) number K827378.

Who is the listed applicant for DIAGNOSTIC X-RAY HV GENERATOR?

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

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Other records listing Technicare 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.

K854340TECHNICARE 720 HPS CT SCANNERK852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEMK844293AUTO DII MULTI FREQUENCYK844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSK843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-K842777AUTOFOCUS DUAL ELEMENT PROBE

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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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