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FDA 510(k)

PRO-CARE

K-Number: K770997 · 1977-06-20

ApplicantYoung Dental Manufacturing Co. 1, LLC
Decision Date1977-06-20
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRO-CARE is the device name listed in this FDA 510(k) record. The listed applicant is Young Dental Manufacturing Co. 1, LLC. It received FDA 510(k) clearance on 1977-06-20 under 510(k) number K770997. 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 PRO-CARE?

PRO-CARE is a medical device that received FDA 510(k) clearance on 1977-06-20. The listed applicant is Young Dental Manufacturing Co. 1, LLC. The 510(k) number is K770997.

When did PRO-CARE receive FDA 510(k) clearance?

PRO-CARE received FDA 510(k) clearance on 1977-06-20, under 510(k) number K770997.

Who is the listed applicant for PRO-CARE?

The FDA 510(k) record lists Young Dental Manufacturing Co. 1, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-CARE?

The FDA product code for PRO-CARE is JEQ.

Other records listing Young Dental Manufacturing Co. 1, LLC 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.

K241041Silver Fluoride Hypersensitivity VarnishK201127DEFEND Ear-loop Face MasksK171377Young INFINITY Cordless Handpiece SystemK153334Oral-B 5% Sodium Fluoride VarnishK932255YOUNG D'GRANULATORK903284YOUNG PROPHY SYSTEM, PS UNIT

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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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