REDI-SCREEN— 510(k) K000979
Substantially EquivalentRedwood Biotech, Inc.
FDA 510(k) clearance K000979 for REDI-SCREEN, Substantially Equivalent on 2000-04-10. Applicant: Redwood Biotech, Inc.. Device class: 2.
Clearance details
- Applicant
- Redwood Biotech, Inc.
- Product code
- Code LAF
- Device class
- Class 2
- Regulation
- 21 CFR 862.3610
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Sunnyvale, CA, US
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