FDA Device Intelligence
HomeHANS RUDOLPH, INC. › 2460 5 WAY STOPCOCK

2460 5 WAY STOPCOCK

HANS RUDOLPH, INC. · Model 2460 · UDI-DI 00874750009503

BYX Prescription
10
510(k) clearances
505
Adverse events (14 deaths)
1
Recalls
230
Facilities

Description

2460B 5W STCK.187FB 10.5/7.5MM

Recalls

DateFirmReason
2018-08-10A M Systems IncSome of the Disposable Smooth Interior Tubing may pull apart when stretched.

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.