THERAPAX DXT 300 SERIES 3— 510(k) K923584
Substantially EquivalentOldelft Corp. of America
FDA 510(k) clearance K923584 for THERAPAX DXT 300 SERIES 3, Substantially Equivalent on 1993-01-15. Applicant: Oldelft Corp. of America. Device class: 2.
Clearance details
- Applicant
- Oldelft Corp. of America
- Product code
- Code JAD
- Device class
- Class 2
- Regulation
- 21 CFR 892.5900
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fairfax, VA, US
Recent devices under product code JAD
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