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FDA 510(k)

MICRO RSH HIGH SPEED HANDPIECE

K-Number: K935676 · 1995-03-31

Decision Date1995-03-31
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO RSH HIGH SPEED HANDPIECE 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 1995-03-31 under 510(k) number K935676. 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 MICRO RSH HIGH SPEED HANDPIECE?

MICRO RSH HIGH SPEED HANDPIECE is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is Micro Motors, Inc.. The 510(k) number is K935676.

When did MICRO RSH HIGH SPEED HANDPIECE receive FDA 510(k) clearance?

MICRO RSH HIGH SPEED HANDPIECE received FDA 510(k) clearance on 1995-03-31, under 510(k) number K935676.

Who is the listed applicant for MICRO RSH HIGH SPEED HANDPIECE?

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 MICRO RSH HIGH SPEED HANDPIECE?

The FDA product code for MICRO RSH HIGH SPEED HANDPIECE 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

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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