HIGH FREQUENCY NEEDLE-TYPE EPILATOR
K-Number: K864291 · 1986-12-24
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Device Summary
Frequently Asked Questions
What is the HIGH FREQUENCY NEEDLE-TYPE EPILATOR?
HIGH FREQUENCY NEEDLE-TYPE EPILATOR is a medical device that received FDA 510(k) clearance on 1986-12-24. The listed applicant is Multi-Channel Epilator. The 510(k) number is K864291.
When did HIGH FREQUENCY NEEDLE-TYPE EPILATOR receive FDA 510(k) clearance?
HIGH FREQUENCY NEEDLE-TYPE EPILATOR received FDA 510(k) clearance on 1986-12-24, under 510(k) number K864291.
Who is the listed applicant for HIGH FREQUENCY NEEDLE-TYPE EPILATOR?
The FDA 510(k) record lists Multi-Channel Epilator as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIGH FREQUENCY NEEDLE-TYPE EPILATOR?
The FDA product code for HIGH FREQUENCY NEEDLE-TYPE EPILATOR is KCW.
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: KCW)
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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