UCA GEL PRODUCT REFORMAULATION— 510(k) K802649
Substantially EquivalentVanaray Laboratories, Inc.
FDA 510(k) clearance K802649 for UCA GEL PRODUCT REFORMAULATION, Substantially Equivalent on 1980-11-12. Applicant: Vanaray Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Vanaray Laboratories, Inc.
- Product code
- Code GYB
- Device class
- Class 2
- Regulation
- 21 CFR 882.1275
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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