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FDA 510(k)

EPILATION NEEDLE

K-Number: K894771 · 1989-08-21

ApplicantPrecision Electrolysis Needles, Inc.
Decision Date1989-08-21
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EPILATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Electrolysis Needles, Inc.. It received FDA 510(k) clearance on 1989-08-21 under 510(k) number K894771. 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 EPILATION NEEDLE?

EPILATION NEEDLE is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Precision Electrolysis Needles, Inc.. The 510(k) number is K894771.

When did EPILATION NEEDLE receive FDA 510(k) clearance?

EPILATION NEEDLE received FDA 510(k) clearance on 1989-08-21, under 510(k) number K894771.

Who is the listed applicant for EPILATION NEEDLE?

The FDA 510(k) record lists Precision Electrolysis Needles, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPILATION NEEDLE?

The FDA product code for EPILATION NEEDLE 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.

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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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