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FDA 510(k)

TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE

K-Number: K043498 · 2005-02-16

Decision Date2005-02-16
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2005-02-16 under 510(k) number K043498. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE?

TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE is a medical device that received FDA 510(k) clearance on 2005-02-16. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K043498.

When did TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE receive FDA 510(k) clearance?

TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE received FDA 510(k) clearance on 2005-02-16, under 510(k) number K043498.

Who is the listed applicant for TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE?

The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL HANDPIECE?

The FDA product code for TWIN POWER TURBINE HIGH SPEED AIR TURBINE DENTAL 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.

Other records listing J. Morita USA, Inc. 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.

View all 52 devices →

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

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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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