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FDA 510(k)

HIGH FREQUENCY NEEDLE-TYPE EPILATOR

K-Number: K864291 · 1986-12-24

Decision Date1986-12-24
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HIGH FREQUENCY NEEDLE-TYPE EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Multi-Channel Epilator. It received FDA 510(k) clearance on 1986-12-24 under 510(k) number K864291. The device is classified under product code KCW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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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