Home › Beckman Coulter, Inc. › PK7400
PK7400
Beckman Coulter, Inc. · Model B53299 · UDI-DI 14987666543344
KSZ
Prescription
4
510(k) clearances
10,406
Adverse events (6 deaths)
0
Recalls
29
Facilities
Description
PK7400 Automated Microplate System
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.
