EMBA Hourglass Peripheral Embolization Device
K-Number: K171845 · 2017-08-18
Device Summary
Frequently Asked Questions
What is the EMBA Hourglass Peripheral Embolization Device?
EMBA Hourglass Peripheral Embolization Device is a medical device that received FDA 510(k) clearance on 2017-08-18. It is manufactured by Emba Medical Limited. The 510(k) number is K171845.
When was EMBA Hourglass Peripheral Embolization Device approved by the FDA?
EMBA Hourglass Peripheral Embolization Device received FDA 510(k) clearance on 2017-08-18, under approval number K171845.
What company makes EMBA Hourglass Peripheral Embolization Device?
EMBA Hourglass Peripheral Embolization Device is manufactured by Emba Medical Limited.
What is the FDA product code for EMBA Hourglass Peripheral Embolization Device?
The FDA product code for EMBA Hourglass Peripheral Embolization Device is KRD.
Related Clinical Trials
Related PubMed Literature
Related Devices (Code: KRD)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.