FDA 510(k)

DIJI-DENT

K-Number: K781962 · 1978-12-20

Decision Date1978-12-20

Product CodeEFW

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DIJI-DENT is the device name listed in this FDA 510(k) record. The listed applicant is J&J Technologies, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781962. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIJI-DENT?

DIJI-DENT is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is J&J Technologies, Inc.. The 510(k) number is K781962.

When did DIJI-DENT receive FDA 510(k) clearance?

DIJI-DENT received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781962.

Who is the listed applicant for DIJI-DENT?

The FDA 510(k) record lists J&J Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIJI-DENT?

The FDA product code for DIJI-DENT is EFW.

Related Devices (Code: EFW)

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.

K130186DENTEK EASY BRUSH WITH FLUORIDEDen Tek Oral Care, Inc.K121165BEAM BRUSH/BEAM APPBeam Technologies, LLC K102871SILVER CARE ANITBACTERIAL TOOTHBRUSHPiave Spazzolificio S.P.A.K073224ORAL-B SUB-BRAND MANUAL TOOTHBRUSHProcter & Gamble K021383ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIALAgion Technologies, LLC K020776MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTSCoronet Group North America, LLC

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.