ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN— 510(k) K933161
Substantially EquivalentDupont Medical Products
FDA 510(k) clearance K933161 for ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN, Substantially Equivalent on 1993-10-07. Applicant: Dupont Medical Products.
Clearance details
- Applicant
- Dupont Medical Products
- Product code
- Code EAM
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.