FDA 510(k)

EPILATOR, ELECTRONIC MODEL SE-2

K-Number: K780076 · 1978-01-24

Decision Date1978-01-24

Product CodeKCW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

EPILATOR, ELECTRONIC MODEL SE-2 is the device name listed in this FDA 510(k) record. The listed applicant is R. A. Fischer Co. Corp.. It received FDA 510(k) clearance on 1978-01-24 under 510(k) number K780076. 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 EPILATOR, ELECTRONIC MODEL SE-2?

EPILATOR, ELECTRONIC MODEL SE-2 is a medical device that received FDA 510(k) clearance on 1978-01-24. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K780076.

When did EPILATOR, ELECTRONIC MODEL SE-2 receive FDA 510(k) clearance?

EPILATOR, ELECTRONIC MODEL SE-2 received FDA 510(k) clearance on 1978-01-24, under 510(k) number K780076.

Who is the listed applicant for EPILATOR, ELECTRONIC MODEL SE-2?

The FDA 510(k) record lists R. A. Fischer Co. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPILATOR, ELECTRONIC MODEL SE-2?

The FDA product code for EPILATOR, ELECTRONIC MODEL SE-2 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing R. A. Fischer Co. Corp. as applicant

K964208MD-1A GALVANIC UNIT K954031COMPU-BLEND EPILATOR K895365MD-2 IONTOPHORESIS UNIT K893389MODEL SE-5 EPILATOR K884079MODEL CBX EPILATOR K871372CB-7 ELECTRONIC EPILATOR

View all 13 devices →

Related Devices (Code: KCW)

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 ROYALEInstantron K943396THE 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.