ADDED USE CLAIM FOR DUPONT ACA BETA-2-MICROGLOBULIN TEST PACK— 510(k) K933648
Substantially EquivalentDupont Medical Products
FDA 510(k) clearance K933648 for ADDED USE CLAIM FOR DUPONT ACA BETA-2-MICROGLOBULIN TEST PACK, Substantially Equivalent on 1993-09-24. Applicant: Dupont Medical Products. Device class: 2.
Clearance details
- Applicant
- Dupont Medical Products
- Product code
- Code JZG
- Device class
- Class 2
- Regulation
- 21 CFR 866.5630
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
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