FDA 510(k)

NEY VIBRATOR

K-Number: K761101 · 1976-12-02

Decision Date1976-12-02

Product Code

DecisionSubstantially Equivalent

Device Summary

NEY VIBRATOR 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 K761101. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEY VIBRATOR?

NEY VIBRATOR 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 K761101.

When did NEY VIBRATOR receive FDA 510(k) clearance?

NEY VIBRATOR received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761101.

Who is the listed applicant for NEY VIBRATOR?

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

Related Clinical Trials

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.

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Other records listing Deringer-Ney, Inc. as applicant

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