FDA Device Intelligence
Home › REMEL, INC. › ACT II Transport PK/10

ACT II Transport PK/10

REMEL, INC. · Model R124101 · UDI-DI 00842558116426

JSL
8
510(k) clearances
54
Adverse events
0
Recalls
9
Facilities

Description

ACT II Dual

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.