CURAMED 402— 510(k) K850573
Substantially EquivalentFluidotherapy Corp.
FDA 510(k) clearance K850573 for CURAMED 402, Substantially Equivalent on 1985-05-17. Applicant: Fluidotherapy Corp.. Device class: 2.
Clearance details
- Applicant
- Fluidotherapy Corp.
- Product code
- Code IMJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
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