MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100
K-Number: K022535 · 2002-10-22
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Device Summary
Frequently Asked Questions
What is the MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100?
MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Microtech. The 510(k) number is K022535.
When did MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 receive FDA 510(k) clearance?
MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 received FDA 510(k) clearance on 2002-10-22, under 510(k) number K022535.
Who is the listed applicant for MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100?
The FDA 510(k) record lists Microtech as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100?
The FDA product code for MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 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.
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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