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FDA 510(k)

FLEXIE THE COPPER SHANK NEEDLE

K-Number: K874891 · 1988-01-07

ApplicantSkin Deep, Inc.
Decision Date1988-01-07
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLEXIE THE COPPER SHANK NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Skin Deep, Inc.. It received FDA 510(k) clearance on 1988-01-07 under 510(k) number K874891. 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 FLEXIE THE COPPER SHANK NEEDLE?

FLEXIE THE COPPER SHANK NEEDLE is a medical device that received FDA 510(k) clearance on 1988-01-07. The listed applicant is Skin Deep, Inc.. The 510(k) number is K874891.

When did FLEXIE THE COPPER SHANK NEEDLE receive FDA 510(k) clearance?

FLEXIE THE COPPER SHANK NEEDLE received FDA 510(k) clearance on 1988-01-07, under 510(k) number K874891.

Who is the listed applicant for FLEXIE THE COPPER SHANK NEEDLE?

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

What is the FDA product code for FLEXIE THE COPPER SHANK NEEDLE?

The FDA product code for FLEXIE THE COPPER SHANK 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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Other records listing Skin Deep, Inc. as applicant

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.

K911983WIZARD STERILIZED ELECTROEPILATION NEEDLE

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

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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