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FDA 510(k)

STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION

K-Number: K952611 · 1995-10-18

ApplicantSterex Electrolysis Intl., Ltd.
Decision Date1995-10-18
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION is the device name listed in this FDA 510(k) record. The listed applicant is Sterex Electrolysis Intl., Ltd.. It received FDA 510(k) clearance on 1995-10-18 under 510(k) number K952611. 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 STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION?

STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Sterex Electrolysis Intl., Ltd.. The 510(k) number is K952611.

When did STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION receive FDA 510(k) clearance?

STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION received FDA 510(k) clearance on 1995-10-18, under 510(k) number K952611.

Who is the listed applicant for STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION?

The FDA 510(k) record lists Sterex Electrolysis Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION?

The FDA product code for STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION 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.K945192HAIR REMOVAL SYSTEML.P. Systems Corp.K943928APILUS ELECTROPILDectro Intl., Inc.K943398THE BLENDTONE ROYALEInstantronK943396THE ELITE SPECTRUMInstantronK943399THE SS-99Instantron

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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