Supermax Automatic X-Ray Processor
FDA 510(k) K760905 · General Electric Co.
510(k) numberK760905
Submission
- Device name
- Supermax Automatic X-Ray Processor
- Applicant
- General Electric Co.
Mchenry, IL, US - Received
- October 26, 1976
- Decision date
- November 19, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Supermax Automatic X-Ray Processor cleared by the FDA?
Supermax Automatic X-Ray Processor (K760905) received a 510(k) decision of Substantially Equivalent on November 19, 1976, 24 days after the submission was received.
What is the product code of K760905?
The FDA product code is IXW – Processor, Radiographic-Film, Automatic, a Class II (moderate risk) device regulated under 21 CFR 892.1900.