ELECTRIC TOOTH-BRUSH
K-Number: K931360 · 1993-07-13
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Device Summary
Frequently Asked Questions
What is the ELECTRIC TOOTH-BRUSH?
ELECTRIC TOOTH-BRUSH is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is U.S. Dentek Corp.. The 510(k) number is K931360.
When did ELECTRIC TOOTH-BRUSH receive FDA 510(k) clearance?
ELECTRIC TOOTH-BRUSH received FDA 510(k) clearance on 1993-07-13, under 510(k) number K931360.
Who is the listed applicant for ELECTRIC TOOTH-BRUSH?
The FDA 510(k) record lists U.S. Dentek Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRIC TOOTH-BRUSH?
The FDA product code for ELECTRIC TOOTH-BRUSH 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.
Other records listing U.S. Dentek 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.
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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