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FDA 510(k)

DYNATORQ DENTAL HANDPIECE ATTACHMENTS

K-Number: K896876 · 1990-03-07

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

Device Summary

DYNATORQ DENTAL HANDPIECE 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 K896876. 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 DYNATORQ DENTAL HANDPIECE ATTACHMENTS?

DYNATORQ DENTAL HANDPIECE 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 K896876.

When did DYNATORQ DENTAL HANDPIECE ATTACHMENTS receive FDA 510(k) clearance?

DYNATORQ DENTAL HANDPIECE ATTACHMENTS received FDA 510(k) clearance on 1990-03-07, under 510(k) number K896876.

Who is the listed applicant for DYNATORQ DENTAL HANDPIECE 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 DYNATORQ DENTAL HANDPIECE ATTACHMENTS?

The FDA product code for DYNATORQ DENTAL HANDPIECE 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

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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