C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST— 510(k) K962019
Substantially EquivalentTeco Diagnostics
FDA 510(k) clearance K962019 for C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST, Substantially Equivalent on 1996-11-25. Applicant: Teco Diagnostics. Device class: 2.
Clearance details
- Applicant
- Teco Diagnostics
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Placentia, CA, US
Recent devices under product code DCK
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