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FDA 510(k)

HAIR REMOVAL SYSTEM

K-Number: K945192 · 1995-01-12

ApplicantL.P. Systems Corp.
Decision Date1995-01-12
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HAIR REMOVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is L.P. Systems Corp.. It received FDA 510(k) clearance on 1995-01-12 under 510(k) number K945192. 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 HAIR REMOVAL SYSTEM?

HAIR REMOVAL SYSTEM is a medical device that received FDA 510(k) clearance on 1995-01-12. The listed applicant is L.P. Systems Corp.. The 510(k) number is K945192.

When did HAIR REMOVAL SYSTEM receive FDA 510(k) clearance?

HAIR REMOVAL SYSTEM received FDA 510(k) clearance on 1995-01-12, under 510(k) number K945192.

Who is the listed applicant for HAIR REMOVAL SYSTEM?

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

What is the FDA product code for HAIR REMOVAL SYSTEM?

The FDA product code for HAIR REMOVAL SYSTEM 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing L.P. Systems Corp. 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.

K820650LPS 1118

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.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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