LeadCare® Blood Lead Test Kit
by Magellan Diagnostics, Inc. United States GUDID
Product code DOF
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850355006154 | Date19 Sep 2016 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-0285-2019
Defect with the calibration button for lot 1808M. Level 1 and Level 2 Quality Control (QC) values will generate results of HIGH (>65 g/dL). Results for patient testing with this lot will be displayed as HIGH.
-
- Terminated Z-2225-2017
Underestimates the lead concentration of venous blood samples when the sample is analyzed with the LeadCare systems
-
- Terminated Z-0914-05
Lead test results may be reported lower than the actual value
Specification
- Generic Name
- Lead (Pb) analyser IVD
- Model / Ref / Catalog
- LeadCare®, 70-2233
- Primary DI / UDI-DI
- 00850355006154
- 510(k) Number
- FDA Product Code
- DOF
- GMDN Term
- Lead (Pb) analyser IVD
- Device Class
- Class II
- Regulation Number
- 862.3550
- Commercial Distribution
- In Commercial Distribution
Other devices from Magellan Diagnostics, Inc.
Properties & raw data
Show properties, registry sources and raw records
Other properties (9)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 242194bf-97c1-43d8-81af-787fe7813306