FRESENIUS PD+ EXCHANGE DEVICE— 510(k) K915634
Substantially EquivalentFresenius USA, Inc.
FDA 510(k) clearance K915634 for FRESENIUS PD+ EXCHANGE DEVICE, Substantially Equivalent on 1993-07-01. Applicant: Fresenius USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Fresenius USA, Inc.
- Product code
- Code EKX
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
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