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FDA 510(k)

DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP

K-Number: K903298 · 1991-04-16

Decision Date1991-04-16
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP 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 1991-04-16 under 510(k) number K903298. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP?

DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Micro Motors, Inc.. The 510(k) number is K903298.

When did DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP receive FDA 510(k) clearance?

DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP received FDA 510(k) clearance on 1991-04-16, under 510(k) number K903298.

Who is the listed applicant for DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP?

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 DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP?

The FDA product code for DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP is ELC.

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: ELC)

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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