GAMBRO PERITONEAL DIALYSIS MONITOR— 510(k) K802831
Substantially EquivalentGambro, Inc.
FDA 510(k) clearance K802831 for GAMBRO PERITONEAL DIALYSIS MONITOR, Substantially Equivalent on 1980-12-18. Applicant: Gambro, Inc.. Device class: 2.
Clearance details
- Applicant
- Gambro, Inc.
- Product code
- Code KPF
- Device class
- Class 2
- Regulation
- 21 CFR 876.5630
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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