FDA 510(k)

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60

K-Number: K032081 · 2003-07-24

Decision Date2003-07-24

Product CodeEIH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America. It received FDA 510(k) clearance on 2003-07-24 under 510(k) number K032081. 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 KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60?

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 is a medical device that received FDA 510(k) clearance on 2003-07-24. The listed applicant is Kavo America. The 510(k) number is K032081.

When did KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 receive FDA 510(k) clearance?

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 received FDA 510(k) clearance on 2003-07-24, under 510(k) number K032081.

Who is the listed applicant for KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60?

The FDA 510(k) record lists Kavo America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60?

The FDA product code for KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 is EIH.

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Other records listing Kavo America as applicant

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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.