PULSE ELECTRIC TOOTHBRUSH
K-Number: K933829 · 1993-12-13
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Device Summary
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
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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