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FDA 510(k)

DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST

K-Number: K812362 · 1981-11-20

ApplicantJdm Commodities
Decision Date1981-11-20
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST is the device name listed in this FDA 510(k) record. The listed applicant is Jdm Commodities. It received FDA 510(k) clearance on 1981-11-20 under 510(k) number K812362. 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 DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST?

DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is Jdm Commodities. The 510(k) number is K812362.

When did DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST receive FDA 510(k) clearance?

DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST received FDA 510(k) clearance on 1981-11-20, under 510(k) number K812362.

Who is the listed applicant for DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST?

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

What is the FDA product code for DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST?

The FDA product code for DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST is EFW.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Jdm Commodities 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.

K812364PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTEK812361PORTABLE TOOTHBRUSH KIT (NO SAMPLE)K812363DISP. TOOTHBRUSH W/TOOTHPASTE ATTACHED

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, LLCK102871SILVER CARE ANITBACTERIAL TOOTHBRUSHPiave Spazzolificio S.P.A.K073224ORAL-B SUB-BRAND MANUAL TOOTHBRUSHProcter & GambleK021383ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIALAgion Technologies, LLCK020776MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTSCoronet Group North America, LLC

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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