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FDA 510(k)

HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR

K-Number: K926154 · 1994-03-04

Decision Date1994-03-04
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR is the device name listed in this FDA 510(k) record. The listed applicant is Dabi-Atlante America Corp.. It received FDA 510(k) clearance on 1994-03-04 under 510(k) number K926154. 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 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

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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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