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FDA 510(k)

EMBA Hourglass Peripheral Embolization Device

K-Number: K171845 · 2017-08-18

Decision Date2017-08-18
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EMBA Hourglass Peripheral Embolization Device is a medical device manufactured by Emba Medical Limited. It received FDA 510(k) clearance on 2017-08-18 under approval number K171845. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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