FASTTECH SYSTEM II— 510(k) K913892
Substantially Equivalent3M Diagnostic Systems, Inc.
FDA 510(k) clearance K913892 for FASTTECH SYSTEM II, Substantially Equivalent on 1991-10-02. Applicant: 3M Diagnostic Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- 3M Diagnostic Systems, Inc.
- Product code
- Code DHB
- Device class
- Class 2
- Regulation
- 21 CFR 866.5750
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
Recent devices under product code DHB
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