ROTOLUX, SELECTOLUX, SHUTTERVUE— 510(k) K922079
Substantially EquivalentAmerican Medical Sales, Inc.
FDA 510(k) clearance K922079 for ROTOLUX, SELECTOLUX, SHUTTERVUE, Substantially Equivalent on 1992-06-16. Applicant: American Medical Sales, Inc.. Device class: 1.
Clearance details
- Applicant
- American Medical Sales, Inc.
- Product code
- Code IXC
- Device class
- Class 1
- Regulation
- 21 CFR 892.1890
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Culver City, CA, US
Recent devices under product code IXC
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