HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR
K-Number: K926154 · 1994-03-04
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Device Summary
Frequently Asked Questions
What is the HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR?
HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR is a medical device that received FDA 510(k) clearance on 1994-03-04. The listed applicant is Dabi-Atlante America Corp.. The 510(k) number is K926154.
When did HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR receive FDA 510(k) clearance?
HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR received FDA 510(k) clearance on 1994-03-04, under 510(k) number K926154.
Who is the listed applicant for HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR?
The FDA 510(k) record lists Dabi-Atlante America Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR?
The FDA product code for HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-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 Dabi-Atlante America Corp. 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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