ENFLOW IV FLUID WARMER INSULATED STRAP— 510(k) K130867
Substantially EquivalentVital Signs, Inc., A GE Healthcare Company
FDA 510(k) clearance K130867 for ENFLOW IV FLUID WARMER INSULATED STRAP, Substantially Equivalent on 2013-06-14. Applicant: Vital Signs, Inc., A GE Healthcare Company. Device class: 2.
Clearance details
- Applicant
- Vital Signs, Inc., A GE Healthcare Company
- Product code
- Code LGZ
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Totowa, NJ, US
Recent devices under product code LGZ
view allMore clearances from Vital Signs, Inc., A GE Healthcare Company
view allAdverse events under product code LGZ
product code LGZ- Death
- 16
- Malfunction
- 5,916
- Other
- 1
- Total
- 5,933
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 K130867
K-number listed on FDA's recall record- Z-1385-2019 — enFlow Disposable Cartridge, used for intravenous warming therapy with fluid and blood solutions.
- Z-1386-2019 — enFlow Disposable Cartridge with IV Extension Set, used for intravenous warming therapy with fluid and blood solutions.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K130867.
Data sourced from openFDA. This site is unofficial and independent of the FDA.