Proact, Ltd.

Proact, Ltd. holds 5 FDA 510(k) medical device clearances, first cleared 1990, most recent 1994.

Top product codes for Proact, Ltd.

FCG — Gastroenterology, Urology3 devices
KNW — Gastroenterology, Urology1 device
LWE — Unknown1 device

Recent clearances by Proact, Ltd.

K941256 — QUICK CORE IICode KNW·1994-07-13
K926559 — PROACT BIOPSY NEEDLE ENCHANCEMENTSCode FCG·1993-03-22
K913306 — BONE-TEMNO/STERNUM-TEMNOCode LWE·1991-11-01
K902320 — BAUER FLEXI-TEMNO BIOPSY NEEDLECode FCG·1990-10-01
K902319 — BAUER TEMNO BIOPSY NEEDLECode FCG·1990-09-06

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