BALLET STERILE DISPOSABLE ELECTROLYSIS— 510(k) K883892

Name: FDA 510(k) clearance K883892
Creator: U.S. Food and Drug Administration
Published: 1988-10-20

Substantially Equivalent

Synoptic Products

FDA 510(k) clearance K883892 for BALLET STERILE DISPOSABLE ELECTROLYSIS, Substantially Equivalent on 1988-10-20. Applicant: Synoptic Products. Device class: 1.

Clearance details

Applicant: Synoptic Products
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1988-09-14
Decision date: 1988-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brookline, MA, US

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Recent devices under product code KCW

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K954031 — COMPU-BLEND EPILATOR1996-01-05
K952611 — STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION1995-10-18
K943928 — APILUS ELECTROPIL1995-01-12
K945192 — HAIR REMOVAL SYSTEM1995-01-12
K943396 — THE ELITE SPECTRUM1994-09-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.