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FDA 510(k)

29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM

K-Number: K911068 · 1991-05-15

Decision Date1991-05-15
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM 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 1991-05-15 under 510(k) number K911068. 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 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM?

29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Micro Motors, Inc.. The 510(k) number is K911068.

When did 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM receive FDA 510(k) clearance?

29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM received FDA 510(k) clearance on 1991-05-15, under 510(k) number K911068.

Who is the listed applicant for 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM?

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 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM?

The FDA product code for 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM 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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