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FDA 510(k)

Suglue 3

K-Number: K192992 · 2019-11-05

Applicant3M Deutschland GmbH
Decision Date2019-11-05
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Suglue 3 is a medical device manufactured by 3M Deutschland GmbH. It received FDA 510(k) clearance on 2019-11-05 under approval 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. It is manufactured by 3M Deutschland GmbH. The 510(k) number is K192992.

When was Suglue 3 approved by the FDA?

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

What company makes Suglue 3?

Suglue 3 is manufactured by 3M Deutschland GmbH.

What is the FDA product code for Suglue 3?

The FDA product code for Suglue 3 is EMA.

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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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