GAMBRO CENTRAL WATER TREATMENT SYSTEM CWP 100 - WRO H— 510(k) K974899
Substantially EquivalentGambro Healthcare
FDA 510(k) clearance K974899 for GAMBRO CENTRAL WATER TREATMENT SYSTEM CWP 100 - WRO H, Substantially Equivalent on 1998-09-23. Applicant: Gambro Healthcare. Device class: 2.
Clearance details
- Applicant
- Gambro Healthcare
- Product code
- Code FIP
- Device class
- Class 2
- Regulation
- 21 CFR 876.5665
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lakewood, CO, US
Recent devices under product code FIP
view allMore clearances from Gambro Healthcare
view all- K994390 — GAMBRO POLYFLUX 17R, CAPILLARY DIALYZER/ FILTER
- K990039 — GAMBRO DQM 200
- K982413 — COBE ARYLANE H1, H4, H6 & H9 HEMODIALYZERS/FILTERS
- K982414 — GAMBRO POLYFLUX 11S, 14S, 17S & 21S HEMODIALYZERS/ HEMOFILTERS
- K980386 — HOSPAL MULTIFLOW 100, MULTIFLOW 100 KITS A0 (A0,A0/B AND A0/0), MULTIFLOW 100 KITS B22 (B22,B22/B, & B22/0)
Adverse events under product code FIP
product code FIP- Malfunction
- 490
- Total
- 490
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K974899
K-number listed on FDA's recall record- Z-1563-2014 — Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse osmosis system with the intended use of producing water for dialysis of multiple patients.
- Z-1201-2014 — Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K974899.
Data sourced from openFDA. This site is unofficial and independent of the FDA.