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FDA 510(k)

ORAL SURGERY HANDPIECE AND ATTACHMENTS

K-Number: K896879 · 1990-03-07

Decision Date1990-03-07
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORAL SURGERY HANDPIECE AND ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Micro Motors, Inc.. It received FDA 510(k) clearance on 1990-03-07 under 510(k) number K896879. 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 ORAL SURGERY HANDPIECE AND ATTACHMENTS?

ORAL SURGERY HANDPIECE AND ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1990-03-07. The listed applicant is Micro Motors, Inc.. The 510(k) number is K896879.

When did ORAL SURGERY HANDPIECE AND ATTACHMENTS receive FDA 510(k) clearance?

ORAL SURGERY HANDPIECE AND ATTACHMENTS received FDA 510(k) clearance on 1990-03-07, under 510(k) number K896879.

Who is the listed applicant for ORAL SURGERY HANDPIECE AND ATTACHMENTS?

The FDA 510(k) record lists Micro Motors, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORAL SURGERY HANDPIECE AND ATTACHMENTS?

The FDA product code for ORAL SURGERY HANDPIECE AND ATTACHMENTS 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 Micro Motors, 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.

View all 14 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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