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FDA 510(k)

PULSE ELECTRIC TOOTHBRUSH

K-Number: K933829 · 1993-12-13

Decision Date1993-12-13
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PULSE ELECTRIC TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Dentatech Corp.. It received FDA 510(k) clearance on 1993-12-13 under 510(k) number K933829. 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 PULSE ELECTRIC TOOTHBRUSH?

PULSE ELECTRIC TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Dentatech Corp.. The 510(k) number is K933829.

When did PULSE ELECTRIC TOOTHBRUSH receive FDA 510(k) clearance?

PULSE ELECTRIC TOOTHBRUSH received FDA 510(k) clearance on 1993-12-13, under 510(k) number K933829.

Who is the listed applicant for PULSE ELECTRIC TOOTHBRUSH?

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

What is the FDA product code for PULSE ELECTRIC TOOTHBRUSH?

The FDA product code for PULSE ELECTRIC 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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