Sircam 106
FDA 510(k) K792394 · Siemens Corp.
510(k) numberK792394
Submission
- Device name
- Sircam 106
- Applicant
- Siemens Corp.
Mchenry, IL, US - Received
- November 26, 1979
- Decision date
- December 20, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Sircam 106 cleared by the FDA?
Sircam 106 (K792394) received a 510(k) decision of Substantially Equivalent on December 20, 1979, 24 days after the submission was received.
What is the product code of K792394?
The FDA product code is IZJ – Camera, X-Ray, Fluorographic, Cine Or Spot, a Class II (moderate risk) device regulated under 21 CFR 892.1620.