DEPILATORY, ELECTRONIC— 510(k) K772322

Substantially Equivalent

Dura Corp., The

FDA 510(k) clearance K772322 for DEPILATORY, ELECTRONIC, Substantially Equivalent on 1978-01-03. Applicant: Dura Corp., The. Device class: 1.

Clearance details

Applicant: Dura Corp., The
Product code: Code KCX
Device class: Class 1
Regulation: 21 CFR 878.5360
Advisory panel: General, Plastic Surgery
Date received: 1977-12-19
Decision date: 1978-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCX

K973773 — DAPELLE HAIR REMOVER1997-12-17
K973340 — TWEEZER-TYPE EPILATOR1997-12-03
K973174 — SONIQUE HAIR REMOVER1997-10-30
K973179 — FEMINIQUE SONIC HAIR REMOVER1997-10-30
K972695 — FINALLY FREE1997-10-22

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