Sightline Technologies , Ltd.

Sightline Technologies , Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2000, most recent 2004.

Top product codes for Sightline Technologies , Ltd.

FER — Gastroenterology, Urology2 devices
FDF — Gastroenterology, Urology1 device

Recent clearances by Sightline Technologies , Ltd.

K032688 — COLONOSIGHT MODEL 510BCode FDF·2004-03-05
K011825 — RECTOSIGHT RS300-04; AND PROTOSIGHT PS300-04 DEVICECode FER·2001-07-11
K994130 — RECTOSIGHT RS 300-04Code FER·2000-06-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.