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FDA 510(k)

mollosil plus

K-Number: K162654 · 2017-03-13

ApplicantDetax GmbH & Co. KG
Decision Date2017-03-13
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

mollosil plus is a medical device manufactured by Detax GmbH & Co. KG. It received FDA 510(k) clearance on 2017-03-13 under approval number K162654. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the mollosil plus?

mollosil plus is a medical device that received FDA 510(k) clearance on 2017-03-13. It is manufactured by Detax GmbH & Co. KG. The 510(k) number is K162654.

When was mollosil plus approved by the FDA?

mollosil plus received FDA 510(k) clearance on 2017-03-13, under approval number K162654.

What company makes mollosil plus?

mollosil plus is manufactured by Detax GmbH & Co. KG.

What is the FDA product code for mollosil plus?

The FDA product code for mollosil plus is EBI.

Other Devices by Detax GmbH & Co. KG

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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.

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