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FDA 510(k)

EPILATOR, EASE-MULTI-MODE

K-Number: K781147 · 1978-10-10

ApplicantGreenleaf-Carter Enterprises, Inc.
Decision Date1978-10-10
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EPILATOR, EASE-MULTI-MODE is the device name listed in this FDA 510(k) record. The listed applicant is Greenleaf-Carter Enterprises, Inc.. It received FDA 510(k) clearance on 1978-10-10 under 510(k) number K781147. 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 EPILATOR, EASE-MULTI-MODE?

EPILATOR, EASE-MULTI-MODE is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Greenleaf-Carter Enterprises, Inc.. The 510(k) number is K781147.

When did EPILATOR, EASE-MULTI-MODE receive FDA 510(k) clearance?

EPILATOR, EASE-MULTI-MODE received FDA 510(k) clearance on 1978-10-10, under 510(k) number K781147.

Who is the listed applicant for EPILATOR, EASE-MULTI-MODE?

The FDA 510(k) record lists Greenleaf-Carter Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPILATOR, EASE-MULTI-MODE?

The FDA product code for EPILATOR, EASE-MULTI-MODE is KCW.

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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.

K954031COMPU-BLEND EPILATORR. A. Fischer Co. Corp.K952611STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATIONSterex Electrolysis Intl., Ltd.K945192HAIR REMOVAL SYSTEML.P. Systems Corp.K943928APILUS ELECTROPILDectro Intl., Inc.K943398THE BLENDTONE ROYALEInstantronK943396THE ELITE SPECTRUMInstantron

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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