GENERATOR, HIGH VOLT, X-RAY, MPX100/125
K-Number: K802551 · 1980-12-02
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Device Summary
Frequently Asked Questions
What is the GENERATOR, HIGH VOLT, X-RAY, MPX100/125?
GENERATOR, HIGH VOLT, X-RAY, MPX100/125 is a medical device that received FDA 510(k) clearance on 1980-12-02. The listed applicant is General Electric Co.. The 510(k) number is K802551.
When did GENERATOR, HIGH VOLT, X-RAY, MPX100/125 receive FDA 510(k) clearance?
GENERATOR, HIGH VOLT, X-RAY, MPX100/125 received FDA 510(k) clearance on 1980-12-02, under 510(k) number K802551.
Who is the listed applicant for GENERATOR, HIGH VOLT, X-RAY, MPX100/125?
The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENERATOR, HIGH VOLT, X-RAY, MPX100/125?
The FDA product code for GENERATOR, HIGH VOLT, X-RAY, MPX100/125 is IZO.
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.
Other records listing General Electric Co. 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.
Related Devices (Code: IZO)
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.
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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