ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE
K-Number: K113222 · 2012-02-23
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Device Summary
Frequently Asked Questions
What is the ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE?
ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE is a medical device that received FDA 510(k) clearance on 2012-02-23. The listed applicant is Nakamura Dental Handpiece Mfg. Co., Ltd.. The 510(k) number is K113222.
When did ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE receive FDA 510(k) clearance?
ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE received FDA 510(k) clearance on 2012-02-23, under 510(k) number K113222.
Who is the listed applicant for ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE?
The FDA 510(k) record lists Nakamura Dental Handpiece Mfg. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE?
The FDA product code for ND LOWSPEED AIRMOTOR,ND HIGHSPEED AIRTURBINE HANDPIECE 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.
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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