IMMULITE/IMMULITE 1000 PROGESTERONE CALIBRATION VERIFICATION (CVM)— 510(k) K103683
Substantially EquivalentSiemens Healthcare Diagnostics
FDA 510(k) clearance K103683 for IMMULITE/IMMULITE 1000 PROGESTERONE CALIBRATION VERIFICATION (CVM), Substantially Equivalent on 2011-04-28. Applicant: Siemens Healthcare Diagnostics. Device class: 1.
Clearance details
- Applicant
- Siemens Healthcare Diagnostics
- Product code
- Code JJX
- Device class
- Class 1
- Regulation
- 21 CFR 862.1660
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Tarrytown, NY, US
Recent devices under product code JJX
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Adverse events under product code JJX
product code JJX- Other
- 2
- Total
- 2
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.