FDA Device Intelligence
Home › Hausmann Enterprises, LLC › RACK+WT,5569,5505(2),5581 (4 PC)

RACK+WT,5569,5505(2),5581 (4 PC)

Hausmann Enterprises, LLC · Model 5569-100 · UDI-DI 00840314806352

IOD
10
510(k) clearances
169
Adverse events
0
Recalls
107
Facilities

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.