Pentax Medical of America, Inc.

Pentax Medical of America, Inc. holds 2 FDA 510(k) medical device clearances, cleared in 2018.

Top product codes for Pentax Medical of America, Inc.

FDF — Gastroenterology, Urology1 device
FDS — Gastroenterology, Urology1 device

Recent clearances by Pentax Medical of America, Inc.

K180285 — PENTAX Medical Video Colonoscope EC34-i10T SeriesCode FDF·2018-10-26
K180292 — PENTAX Video Upper G.I. Scope EG34-i10Code FDS·2018-10-12

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