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FDA 510(k)

NEY-LITE

K-Number: K761102 · 1976-12-02

ApplicantDeringer-Ney, Inc.
Decision Date1976-12-02
Product Code
DecisionSubstantially Equivalent

Device Summary

NEY-LITE 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 1976-12-02 under 510(k) number K761102. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEY-LITE?

NEY-LITE is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K761102.

When did NEY-LITE receive FDA 510(k) clearance?

NEY-LITE received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761102.

Who is the listed applicant for NEY-LITE?

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

Other records listing Deringer-Ney, Inc. as applicant

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.

K933178GDC 3509K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

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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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