FDA Device Intelligence
Home › SPACELABS HEALTHCARE (WASHINGTON), INC › SPACELABS HEALTHCARE

SPACELABS HEALTHCARE

SPACELABS HEALTHCARE (WASHINGTON), INC · Model ARIA; SUPPLY · UDI-DI 30841522123041

DSH Prescription
10
510(k) clearances
972
Adverse events (6 deaths)
0
Recalls
57
Facilities

Description

KIT,HOOK-UP,CASE OF 20,ARIA

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.