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ES102EX
KOVEN TECHNOLOGY, INC. · Model ES102EX · UDI-DI 00894912002173
KNG
Prescription
10
510(k) clearances
32
Adverse events (2 deaths)
1
Recalls
31
Facilities
Description
Fetal Echosounder Doppler
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-10-06 | CooperSurgical, Inc. | The 2MHZ prove was incorrectlhttp://cts.fda.gov/division-tracking/images/trash.pngy labeled as a 3MHZ probe |
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