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FDA 510(k)

MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH

K-Number: K903510 · 1990-09-10

Decision Date1990-09-10
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Helm Toy Corp.. It received FDA 510(k) clearance on 1990-09-10 under 510(k) number K903510. 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 MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH?

MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1990-09-10. The listed applicant is Helm Toy Corp.. The 510(k) number is K903510.

When did MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH receive FDA 510(k) clearance?

MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH received FDA 510(k) clearance on 1990-09-10, under 510(k) number K903510.

Who is the listed applicant for MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH?

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

What is the FDA product code for MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH?

The FDA product code for MICKEY/MINNIE MOUSE BATT. OPERATE TOOTHBRUSH is JEQ.

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.

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.

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.

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