FDA Device Intelligence
Home › PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE › Pathway®

Pathway®

PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE · Model 6425 · UDI-DI 00852423006196

KPI Prescription
10
510(k) clearances
26
Adverse events
0
Recalls
41
Facilities

Description

Pathway® Rectal Silicon Pressure Sensor

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.