MODIFIED CRP LATEX TEST— 510(k) K880016
Substantially EquivalentSclavo, Inc.
FDA 510(k) clearance K880016 for MODIFIED CRP LATEX TEST, Substantially Equivalent on 1988-02-25. Applicant: Sclavo, Inc.. Device class: 2.
Clearance details
- Applicant
- Sclavo, Inc.
- 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
- Wayne, NJ, US
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