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FDA 510(k)

NEY EQUI-HINGE

K-Number: K790290 · 1979-04-10

ApplicantDeringer-Ney, Inc.
Decision Date1979-04-10
Product CodeECG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEY EQUI-HINGE 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 1979-04-10 under 510(k) number K790290. The device is classified under product code ECG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEY EQUI-HINGE?

NEY EQUI-HINGE is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K790290.

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

NEY EQUI-HINGE received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790290.

Who is the listed applicant for NEY EQUI-HINGE?

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 NEY EQUI-HINGE?

The FDA product code for NEY EQUI-HINGE is ECG.

Related Clinical Trials

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

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Related Devices (Code: ECG)

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.

K895164EAGLE DSAmerican Sterilizer Co.K843234CITOMAT AUTOCLAVESLic-OrthionK811237MAGNETIC RETENTION UNITUniversiti MalayaK810977ENDODONTIC POST SYSTEMSPreat Corp.K790078BAR & RIDER, SCREWS, TUBESEurodent, Inc.K771266STEAM STERILIZERAmsco Hospital Products Co.

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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