DIGITAL CRADLE— 510(k) K840463
Substantially EquivalentSpectrum X-Ray Corp.
FDA 510(k) clearance K840463 for DIGITAL CRADLE, Substantially Equivalent on 1984-02-21. Applicant: Spectrum X-Ray Corp.. Device class: 1.
Clearance details
- Applicant
- Spectrum X-Ray Corp.
- Product code
- Code KXH
- Device class
- Class 1
- Regulation
- 21 CFR 892.1830
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code KXH
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