DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL— 510(k) K952412
Substantially EquivalentDupont Medical Products
FDA 510(k) clearance K952412 for DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL, Substantially Equivalent on 1995-06-23. Applicant: Dupont Medical Products. Device class: 1.
Clearance details
- Applicant
- Dupont Medical Products
- Product code
- Code DIF
- Device class
- Class 1
- Regulation
- 21 CFR 862.3280
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newark, DE, US
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More clearances from Dupont Medical Products
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