AQ Flex19 Miniprobe

Mauna Kea Has Received 510(K) Clearance From The Us FDA for Its AQ-Flex 19 Miniprobe
May 3, 2013
Mauna Kea Technologies has received 510(k) clearance from the US Food and Drug Administration (FDA) for its AQ-Flex 19 miniprobe. AQ-Flex 19 miniprobe is used to provide real-time optical biopsies during endoscopic ultrasound-guided fine ...

Tags: Mauna Kea Technologies, AQ-Flex19 Miniprobe