REDI-TEST THC— 510(k) K990870
Substantially EquivalentRedwood Biotech, Inc.
FDA 510(k) clearance K990870 for REDI-TEST THC, Substantially Equivalent on 1999-04-27. Applicant: Redwood Biotech, Inc.. Device class: 2.
Clearance details
- Applicant
- Redwood Biotech, Inc.
- Product code
- Code LDJ
- Device class
- Class 2
- Regulation
- 21 CFR 862.3870
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sunnyvale, CA, US
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More clearances from Redwood Biotech, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.