TURBINE, AIR DRIVEN HANDPIECE (2000)
K-Number: K760331 · 1976-08-11
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Device Summary
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.
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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