Radial Travel Spec. Procedures Table
FDA 510(k) K761339 · Xre Corp.
510(k) numberK761339
Submission
- Device name
- Radial Travel Spec. Procedures Table
- Applicant
- Xre Corp.
Walker, MI, US - Received
- December 27, 1976
- Decision date
- January 5, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Radial Travel Spec. Procedures Table cleared by the FDA?
Radial Travel Spec. Procedures Table (K761339) received a 510(k) decision of Substantially Equivalent on January 5, 1977, 9 days after the submission was received.
What is the product code of K761339?
The FDA product code is IZZ – Table, Radiographic, Non-Tilting, Powered, a Class II (moderate risk) device regulated under 21 CFR 892.1980.