REDI-SCREEN— 510(k) K000979

Substantially Equivalent

Redwood Biotech, Inc.

FDA 510(k) clearance K000979 for REDI-SCREEN, Substantially Equivalent on 2000-04-10. Applicant: Redwood Biotech, Inc..

Clearance details

Applicant: Redwood Biotech, Inc.
Product code: Code LAF
Advisory panel: Clinical Toxicology
Date received: 2000-03-27
Decision date: 2000-04-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

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