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FDA 510(k)

PORCELAIN PRIMER

K-Number: K920534 · 1992-03-26

ApplicantConfi-Dental Products Co.
Decision Date1992-03-26
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORCELAIN PRIMER is the device name listed in this FDA 510(k) record. The listed applicant is Confi-Dental Products Co.. It received FDA 510(k) clearance on 1992-03-26 under 510(k) number K920534. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORCELAIN PRIMER?

PORCELAIN PRIMER is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K920534.

When did PORCELAIN PRIMER receive FDA 510(k) clearance?

PORCELAIN PRIMER received FDA 510(k) clearance on 1992-03-26, under 510(k) number K920534.

Who is the listed applicant for PORCELAIN PRIMER?

The FDA 510(k) record lists Confi-Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORCELAIN PRIMER?

The FDA product code for PORCELAIN PRIMER is DYH.

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Other records listing Confi-Dental Products Co. as applicant

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Related Devices (Code: DYH)

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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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