Philips Super CP Family
FDA 510(k) K925844 · Philips Medical Systems, Inc.
510(k) numberK925844
Submission
- Device name
- Philips Super CP Family
- Applicant
- Philips Medical Systems, Inc.
5680 Da Best, NL - Received
- November 18, 1992
- Decision date
- December 28, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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Questions and answers
When was Philips Super CP Family cleared by the FDA?
Philips Super CP Family (K925844) received a 510(k) decision of Substantially Equivalent on December 28, 1992, 40 days after the submission was received.
What is the product code of K925844?
The FDA product code is IZO – Generator, High-Voltage, X-Ray, Diagnostic, a Class I (low risk) device regulated under 21 CFR 892.1700.