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FDA 510(k)

ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH

K-Number: K936076 · 1994-01-26

ApplicantOhio Health Care Products, Inc.
Decision Date1994-01-26
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Health Care Products, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K936076. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH?

ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Ohio Health Care Products, Inc.. The 510(k) number is K936076.

When did ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH receive FDA 510(k) clearance?

ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH received FDA 510(k) clearance on 1994-01-26, under 510(k) number K936076.

Who is the listed applicant for ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH?

The FDA 510(k) record lists Ohio Health Care Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH?

The FDA product code for ORAL EASE AUTOMATIC FLOSSER/POWER BRUSH is JEQ.

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Related Devices (Code: JEQ)

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.

K200881Oral-B iO Test Drive Power Brush Trial Program KitThe Procter & Gamble CompanyK061351ORAL-B SONIC COMPLETEBraun GmbHK061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESBraun GmbHK040416SONICARE ADVANCE TOOTHBRUSH, MODEL 4900Philips Oral Healthcare, Inc.K022900BUTLER GUM VARI-CLEAN POWER TOOTHBRUSHESJohn O. Butler Co.K012914SONICWAVE SONIC PLAQUE REMOVERHomedics, Inc.

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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