ROCHE COBAS ARGOS 5 DIFF— 510(k) K912615
Substantially EquivalentRoche Diagnostic Systems, Inc.
FDA 510(k) clearance K912615 for ROCHE COBAS ARGOS 5 DIFF, Substantially Equivalent on 1991-09-27. Applicant: Roche Diagnostic Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Roche Diagnostic Systems, Inc.
- Product code
- Code GZI
- Device class
- Class 2
- Regulation
- 21 CFR 882.5810
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Montclair, NJ, US
Recent devices under product code GZI
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