29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM
K-Number: K911068 · 1991-05-15
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Device Summary
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.
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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