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FDA 510(k)

COGAN CORP KITS OF DENTAL HAND INSTRUMENTS

K-Number: K915299 · 1992-01-31

ApplicantCogan Corp.
Decision Date1992-01-31
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COGAN CORP KITS OF DENTAL HAND INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Cogan Corp.. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K915299. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COGAN CORP KITS OF DENTAL HAND INSTRUMENTS?

COGAN CORP KITS OF DENTAL HAND INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Cogan Corp.. The 510(k) number is K915299.

When did COGAN CORP KITS OF DENTAL HAND INSTRUMENTS receive FDA 510(k) clearance?

COGAN CORP KITS OF DENTAL HAND INSTRUMENTS received FDA 510(k) clearance on 1992-01-31, under 510(k) number K915299.

Who is the listed applicant for COGAN CORP KITS OF DENTAL HAND INSTRUMENTS?

The FDA 510(k) record lists Cogan Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COGAN CORP KITS OF DENTAL HAND INSTRUMENTS?

The FDA product code for COGAN CORP KITS OF DENTAL HAND INSTRUMENTS is EGG.

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Related Devices (Code: EGG)

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.

K990979STECO-TITANMAGNETICSSteco-System-Technik GmbH & CokgK950259COUPLING DEVICE FOR DENTAL PROSTHESISDr. Joseph E. Grasso, D.D.S.K925700ZEST ANCHOR ADVANCED GENERATIONZest Anchors, Inc.K912435DENTAL CONNECTOR PRECISION ATTACHMENTMetalor Dental USA Corp.K912567CONICAST, INTRACAST, OMECASTMetalor Dental USA Corp.K901928INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACHInterpore Intl.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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