FDA 510(k)

Suglue 3

K-Number: K192992 · 2019-11-05

Decision Date2019-11-05

Product CodeEMA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Suglue 3 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Deutschland GmbH. It received FDA 510(k) clearance on 2019-11-05 under 510(k) number K192992. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Suglue 3?

Suglue 3 is a medical device that received FDA 510(k) clearance on 2019-11-05. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K192992.

When did Suglue 3 receive FDA 510(k) clearance?

Suglue 3 received FDA 510(k) clearance on 2019-11-05, under 510(k) number K192992.

Who is the listed applicant for Suglue 3?

The FDA 510(k) record lists 3M Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Suglue 3?

The FDA product code for Suglue 3 is EMA.

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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.