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FDA 510(k)

HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS)

K-Number: K896878 · 1990-03-08

Decision Date1990-03-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) 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 1990-03-08 under 510(k) number K896878. 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 SYSTEM WITH MOTOR (SEVERAL MODELS)?

HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) is a medical device that received FDA 510(k) clearance on 1990-03-08. The listed applicant is Micro Motors, Inc.. The 510(k) number is K896878.

When did HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) receive FDA 510(k) clearance?

HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) received FDA 510(k) clearance on 1990-03-08, under 510(k) number K896878.

Who is the listed applicant for HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS)?

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 HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS)?

The FDA product code for HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) 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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