Proview (E7015) & Prolink Image Display System
FDA 510(k) K872245 · General Electric Co.
510(k) numberK872245
Submission
- Device name
- Proview (E7015) & Prolink Image Display System
- Applicant
- General Electric Co.
Milwaukee, WI, US - Received
- June 11, 1987
- Decision date
- June 19, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Proview (E7015) & Prolink Image Display System cleared by the FDA?
Proview (E7015) & Prolink Image Display System (K872245) received a 510(k) decision of Substantially Equivalent on June 19, 1987, 8 days after the submission was received.
What is the product code of K872245?
The FDA product code is IXC – Illuminator, Radiographic-Film, a Class I (low risk) device regulated under 21 CFR 892.1890.