FDA Device Intelligence
Home › RAD SOURCE TECHNOLOGIES, INC. › RS

RS

RAD SOURCE TECHNOLOGIES, INC. · Model 3400 · UDI-DI 00860000737005

MOT
1
510(k) clearances
7
Adverse events
2
Recalls
4
Facilities

Description

Blood Irradiator

Recalls

DateFirmReason
2016-05-06BEST THERATRONICS LTD.It was discovered that both the new device and the predicate device failed to comply with performance standard.
2002-06-01Rad-Source Technologies, Inc.The firm completed a cooling system retrofit to preclude overheating and failure.

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.