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FDA 510(k)

CEREC VITABLOCKS MK2

K-Number: K022408 · 2002-09-06

ApplicantB.B.'S Prophy Shop
Decision Date2002-09-06
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEREC VITABLOCKS MK2 is the device name listed in this FDA 510(k) record. The listed applicant is B.B.'S Prophy Shop. It received FDA 510(k) clearance on 2002-09-06 under 510(k) number K022408. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREC VITABLOCKS MK2?

CEREC VITABLOCKS MK2 is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is B.B.'S Prophy Shop. The 510(k) number is K022408.

When did CEREC VITABLOCKS MK2 receive FDA 510(k) clearance?

CEREC VITABLOCKS MK2 received FDA 510(k) clearance on 2002-09-06, under 510(k) number K022408.

Who is the listed applicant for CEREC VITABLOCKS MK2?

The FDA 510(k) record lists B.B.'S Prophy Shop as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEREC VITABLOCKS MK2?

The FDA product code for CEREC VITABLOCKS MK2 is EIH.

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Related Devices (Code: EIH)

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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