REVISED LABELING FOR ABUSCREEN EIA BARBITURATE— 510(k) K874210
Substantially EquivalentRoche Diagnostic Systems, Inc.
FDA 510(k) clearance K874210 for REVISED LABELING FOR ABUSCREEN EIA BARBITURATE, Substantially Equivalent on 1987-11-13. Applicant: Roche Diagnostic Systems, Inc..
Clearance details
- Applicant
- Roche Diagnostic Systems, Inc.
- Product code
- Code DIS
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nutley, NJ, US
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