ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR
K-Number: K974671 · 1998-03-11
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Device Summary
Frequently Asked Questions
What is the ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR?
ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR is a medical device that received FDA 510(k) clearance on 1998-03-11. The listed applicant is Athena Technology, Inc.. The 510(k) number is K974671.
When did ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR receive FDA 510(k) clearance?
ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR received FDA 510(k) clearance on 1998-03-11, under 510(k) number K974671.
Who is the listed applicant for ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR?
The FDA 510(k) record lists Athena Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR?
The FDA product code for ATHENA 20R S TYPE SLOW SPEED HANDPIECE MOTOR 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 Athena Technology, 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.
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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