FDA Device Intelligence
Home › RITE AID CORPORATION › Rite Aid

Rite Aid

RITE AID CORPORATION · Model 8024509 · UDI-DI 00011822001687

NFYNFW
0
510(k) clearances
0
Adverse events
0
Recalls
52
Facilities

Description

Home Drug Test 2 Panel COC/THC

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.