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FDA 510(k)

NU-GLAZE

K-Number: K781935 · 1978-12-20

ApplicantDeringer-Ney, Inc.
Decision Date1978-12-20
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NU-GLAZE is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781935. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-GLAZE?

NU-GLAZE is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K781935.

When did NU-GLAZE receive FDA 510(k) clearance?

NU-GLAZE received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781935.

Who is the listed applicant for NU-GLAZE?

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

What is the FDA product code for NU-GLAZE?

The FDA product code for NU-GLAZE is ELL.

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Other records listing Deringer-Ney, Inc. 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.

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