Home › Device types › PEJ
Salivary Estriol Test
FDA product code PEJ · Class 3 · Unknown
2
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-07-14 | DRG Instruments GmbH | Lower recovery of salivary estradiol levels due to poor differentiation between kit Standard 0 and Standard 1. |
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