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FDA 510(k)

Clean & More

K-Number: K151748 · 2016-03-11

Applicant3M Deutschland GmbH
Decision Date2016-03-11
Product CodePIP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Clean & More 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 2016-03-11 under 510(k) number K151748. The device is classified under product code PIP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Clean & More?

Clean & More is a medical device that received FDA 510(k) clearance on 2016-03-11. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K151748.

When did Clean & More receive FDA 510(k) clearance?

Clean & More received FDA 510(k) clearance on 2016-03-11, under 510(k) number K151748.

Who is the listed applicant for Clean & More?

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 Clean & More?

The FDA product code for Clean & More is PIP.

Other records listing 3M Deutschland GmbH 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

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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