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FDA 510(k)

THE VP500 EPILATOR

K-Number: K931062 · 1993-07-08

ApplicantInstantron
Decision Date1993-07-08
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE VP500 EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Instantron. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K931062. 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 THE VP500 EPILATOR?

THE VP500 EPILATOR is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Instantron. The 510(k) number is K931062.

When did THE VP500 EPILATOR receive FDA 510(k) clearance?

THE VP500 EPILATOR received FDA 510(k) clearance on 1993-07-08, under 510(k) number K931062.

Who is the listed applicant for THE VP500 EPILATOR?

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

What is the FDA product code for THE VP500 EPILATOR?

The FDA product code for THE VP500 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.

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Other records listing Instantron 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.

K943398THE BLENDTONE ROYALEK943399THE SS-99K943396THE ELITE SPECTRUMK941227SHORTWAVE EPILATOR FOR PERMANENT HAIR REMOVALK931063THE ELITE EPILATORK931064THE BLENDTONE EPILATOR

View all 7 devices →

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.K943399THE SS-99InstantronK943398THE BLENDTONE ROYALEInstantron

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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