EURO-COLLINS SOLUTION SETS— 510(k) K884609
Substantially EquivalentFresenius USA, Inc.
FDA 510(k) clearance K884609 for EURO-COLLINS SOLUTION SETS, Substantially Equivalent on 1989-01-26. Applicant: Fresenius USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Fresenius USA, Inc.
- Product code
- Code KDL
- Device class
- Class 2
- Regulation
- 21 CFR 876.5880
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Germany, DE
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