STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION— 510(k) K952611

Name: FDA 510(k) clearance K952611
Creator: U.S. Food and Drug Administration
Published: 1995-10-18

Substantially Equivalent

Sterex Electrolysis Intl., Ltd.

FDA 510(k) clearance K952611 for STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION, Substantially Equivalent on 1995-10-18. Applicant: Sterex Electrolysis Intl., Ltd.. Device class: 1.

Clearance details

Applicant: Sterex Electrolysis Intl., Ltd.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1995-06-07
Decision date: 1995-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Birmingham, GB

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K943928 — APILUS ELECTROPIL1995-01-12
K945192 — HAIR REMOVAL SYSTEM1995-01-12
K943396 — THE ELITE SPECTRUM1994-09-16
K943398 — THE BLENDTONE ROYALE1994-09-16

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