REDI-TEST PCP— 510(k) K991698
Substantially EquivalentRedwood Biotech, Inc.
FDA 510(k) clearance K991698 for REDI-TEST PCP, Substantially Equivalent on 1999-08-25. Applicant: Redwood Biotech, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Redwood Biotech, Inc.
- Product code
- Code LCM
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountian View, CA, US
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