FDA 510(k)

mollosil plus

K-Number: K162654 · 2017-03-13

Decision Date2017-03-13

Product CodeEBI

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

mollosil plus is the device name listed in this FDA 510(k) record. The listed applicant is Detax GmbH & Co. KG. It received FDA 510(k) clearance on 2017-03-13 under 510(k) 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. The listed applicant is Detax GmbH & Co. KG. The 510(k) number is K162654.

When did mollosil plus receive FDA 510(k) clearance?

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

Who is the listed applicant for mollosil plus?

The FDA 510(k) record lists Detax GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for mollosil plus?

The FDA product code for mollosil plus is EBI.

Other records listing Detax GmbH & Co. KG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.