ABUSCREEN RADIOIMMUNOASSAY FOR CANNABI— 510(k) K820391
Substantially EquivalentHoffmann-La Roche, Inc.
FDA 510(k) clearance K820391 for ABUSCREEN RADIOIMMUNOASSAY FOR CANNABI, Substantially Equivalent on 1982-03-08. Applicant: Hoffmann-La Roche, Inc.. Device class: 2.
Clearance details
- Applicant
- Hoffmann-La Roche, Inc.
- Product code
- Code LAT
- Device class
- Class 2
- Regulation
- 21 CFR 862.3870
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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