X-RAY CONTROL & X-RAY HV GENERATOR
K-Number: K770338 · 1977-03-01
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Device Summary
Frequently Asked Questions
What is the X-RAY CONTROL & X-RAY HV GENERATOR?
X-RAY CONTROL & X-RAY HV GENERATOR is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Litton Medical Systems. The 510(k) number is K770338.
When did X-RAY CONTROL & X-RAY HV GENERATOR receive FDA 510(k) clearance?
X-RAY CONTROL & X-RAY HV GENERATOR received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770338.
Who is the listed applicant for X-RAY CONTROL & X-RAY HV GENERATOR?
The FDA 510(k) record lists Litton Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-RAY CONTROL & X-RAY HV GENERATOR?
The FDA product code for X-RAY CONTROL & X-RAY HV GENERATOR 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 Litton Medical Systems 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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