PROACT 1— 510(k) K003909
Substantially EquivalentProact Co.
FDA 510(k) clearance K003909 for PROACT 1, Substantially Equivalent on 2001-06-13. Applicant: Proact Co.. Device class: 2.
Clearance details
- Applicant
- Proact Co.
- Product code
- Code IRP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5650
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mt Pleasant, SC, US
Recent devices under product code IRP
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