FDA 510(k)

COSP2

K-Number: K093721 · 2010-02-19

Decision Date2010-02-19

Product CodeMVL

DecisionSubstantially Equivalent

Device Summary

COSP2 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Espe AG Dental Products. It received FDA 510(k) clearance on 2010-02-19 under 510(k) number K093721. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSP2?

COSP2 is a medical device that received FDA 510(k) clearance on 2010-02-19. The listed applicant is 3M Espe AG Dental Products. The 510(k) number is K093721.

When did COSP2 receive FDA 510(k) clearance?

COSP2 received FDA 510(k) clearance on 2010-02-19, under 510(k) number K093721.

Who is the listed applicant for COSP2?

The FDA 510(k) record lists 3M Espe AG Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COSP2?

The FDA product code for COSP2 is MVL.

Other records listing 3M Espe AG Dental Products 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.

K100908UNICEM HM K100756MALTA K094007UNICEM K091826ELEGANT K090718BELLUS SHADING KIT K080514PECD-01 AND PECD QUICK-01

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Related Devices (Code: MVL)

K254239CyClean CordSS GLOBAL K253797One-StopMediclus Co., Ltd.K243910RetraxilKulzer, LLC K211420Stasis GelBelport Company, Inc., Gingi-Pak K211419Gingi-Aid GelBelport Company, Inc., Gingi-Pak K213149VOCO Retraction PasteVoco GmbH

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.