ESTYLUS ELECTRIC MOTOR SYSTEM
K-Number: K031145 · 2003-07-15
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Device Summary
Frequently Asked Questions
What is the ESTYLUS ELECTRIC MOTOR SYSTEM?
ESTYLUS ELECTRIC MOTOR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-15. The listed applicant is Dentsply Intl.. The 510(k) number is K031145.
When did ESTYLUS ELECTRIC MOTOR SYSTEM receive FDA 510(k) clearance?
ESTYLUS ELECTRIC MOTOR SYSTEM received FDA 510(k) clearance on 2003-07-15, under 510(k) number K031145.
Who is the listed applicant for ESTYLUS ELECTRIC MOTOR SYSTEM?
The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ESTYLUS ELECTRIC MOTOR SYSTEM?
The FDA product code for ESTYLUS ELECTRIC MOTOR SYSTEM is EFB.
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 Dentsply Intl. 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: EFB)
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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