FDA Device Intelligence
Home › MCKESSON MEDICAL-SURGICAL INC. › McKesson

McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 259-SD3V · UDI-DI 10612479277110

KNG Prescription
1
510(k) clearances
32
Adverse events (2 deaths)
1
Recalls
30
Facilities

Description

Doppler no display, No probe.

Recalls

DateFirmReason
2017-10-06CooperSurgical, 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 docs
Data 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.