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FDA 510(k)

TURBINE, AIR DRIVEN HANDPIECE (2000)

K-Number: K760331 · 1976-08-11

Decision Date1976-08-11
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TURBINE, AIR DRIVEN HANDPIECE (2000) is the device name listed in this FDA 510(k) record. The listed applicant is Litton Dental Products. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760331. 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 TURBINE, AIR DRIVEN HANDPIECE (2000)?

TURBINE, AIR DRIVEN HANDPIECE (2000) is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Litton Dental Products. The 510(k) number is K760331.

When did TURBINE, AIR DRIVEN HANDPIECE (2000) receive FDA 510(k) clearance?

TURBINE, AIR DRIVEN HANDPIECE (2000) received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760331.

Who is the listed applicant for TURBINE, AIR DRIVEN HANDPIECE (2000)?

The FDA 510(k) record lists Litton Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURBINE, AIR DRIVEN HANDPIECE (2000)?

The FDA product code for TURBINE, AIR DRIVEN HANDPIECE (2000) 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 Litton Dental Products 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 12 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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