Conversion Contractor Timer Kit
FDA 510(k) K791933 · Advanced Instrument Development, Inc.
510(k) numberK791933
Submission
- Device name
- Conversion Contractor Timer Kit
- Applicant
- Advanced Instrument Development, Inc.
Mchenry, IL, US - Received
- September 27, 1979
- Decision date
- November 13, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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| K954666 | MPH50, MPH65, and MPH80IZO · Traditional | GE Medical Systems | 11/24/1995SE |
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| K950040 | Sii 525 AprIZO · Traditional | Scott Imaging Intl., Inc. | 03/21/1995SE |
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Questions and answers
When was Conversion Contractor Timer Kit cleared by the FDA?
Conversion Contractor Timer Kit (K791933) received a 510(k) decision of Substantially Equivalent on November 13, 1979, 47 days after the submission was received.
What is the product code of K791933?
The FDA product code is IZO – Generator, High-Voltage, X-Ray, Diagnostic, a Class I (low risk) device regulated under 21 CFR 892.1700.