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FDA 510(k)

SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201

K-Number: K852279 · 1985-07-01

ApplicantNorthern Electric Co. Div. of Sunbeam Corp.
Decision Date1985-07-01
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201 is the device name listed in this FDA 510(k) record. The listed applicant is Northern Electric Co. Div. of Sunbeam Corp.. It received FDA 510(k) clearance on 1985-07-01 under 510(k) number K852279. 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 SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201?

SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201 is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Northern Electric Co. Div. of Sunbeam Corp.. The 510(k) number is K852279.

When did SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201 receive FDA 510(k) clearance?

SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201 received FDA 510(k) clearance on 1985-07-01, under 510(k) number K852279.

Who is the listed applicant for SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201?

The FDA 510(k) record lists Northern Electric Co. Div. of Sunbeam Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201?

The FDA product code for SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201 is JEQ.

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Other records listing Northern Electric Co. Div. of Sunbeam Corp. 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.

K860118SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220K851220SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664K852593SUNBEAM DENTAL CARE CENTER, MODEL NO. 6273

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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