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FDA 510(k)

HEANY INDUSTRIES INC DENTAL XIRCONIA

K-Number: K073314 · 2008-02-21

ApplicantHeany Industries, Inc.
Decision Date2008-02-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HEANY INDUSTRIES INC DENTAL XIRCONIA is the device name listed in this FDA 510(k) record. The listed applicant is Heany Industries, Inc.. It received FDA 510(k) clearance on 2008-02-21 under 510(k) number K073314. 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 HEANY INDUSTRIES INC DENTAL XIRCONIA?

HEANY INDUSTRIES INC DENTAL XIRCONIA is a medical device that received FDA 510(k) clearance on 2008-02-21. The listed applicant is Heany Industries, Inc.. The 510(k) number is K073314.

When did HEANY INDUSTRIES INC DENTAL XIRCONIA receive FDA 510(k) clearance?

HEANY INDUSTRIES INC DENTAL XIRCONIA received FDA 510(k) clearance on 2008-02-21, under 510(k) number K073314.

Who is the listed applicant for HEANY INDUSTRIES INC DENTAL XIRCONIA?

The FDA 510(k) record lists Heany Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEANY INDUSTRIES INC DENTAL XIRCONIA?

The FDA product code for HEANY INDUSTRIES INC DENTAL XIRCONIA is EIH.

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Related Devices (Code: EIH)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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