Home › Coopersurgical, Inc. › Summit Doppler
Summit Doppler
Coopersurgical, Inc. · Model L250R-SD2 · UDI-DI 00888937002201
KNG
Prescription
1
510(k) clearances
32
Adverse events (2 deaths)
1
Recalls
31
Facilities
Description
LifeDop 250R Professional with 2.0 MHz Fetal Probe
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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.