Product code KCX— General, Plastic Surgery
TWEEZER-TYPE EPILATOR
- Classification name
- Epilator, High Frequency, Tweezer-Type
- Device class
- Class 1
- Regulation
- 21 CFR 878.5360
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 25
- First cleared
- Most recent
Market context for product code KCX
FDA has cleared devices under product code KCX between 1976 and 1997, filed by 21 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1997
- 1995
- 1992
- 1991
- 1990
- 1985
- 1984
- 1981
- 1980
- 1979
- 1978
- 1977
- 1976
Top applicants under product code KCX
Recent clearances under product code KCX
- K973773 — DAPELLE HAIR REMOVER
- K973340 — TWEEZER-TYPE EPILATOR
- K973174 — SONIQUE HAIR REMOVER
- K973179 — FEMINIQUE SONIC HAIR REMOVER
- K972695 — FINALLY FREE
- K970338 — TWEEZER-TYPE EPILATOR
- K935706 — EPI 2
- K943872 — COMMANDER MARK II HAIR REMOVAL SYSTEM
- K952117 — EPILATOR
- K915845 — HAIR TRONICS MODEL HT8000
- K905125 — GUARANTY HAIR REMOVAL SYSTEM
- K892514 — AHRS EPILATOR 629
- K851413 — EPILATOR 8500
- K843734 — NEMDI
- K843735 — SOFTEPIL
- K770791 — DEPILATOR, DERMA-I & DERMA-II
- K802513 — DPA 207 PERSONAL
- K782119 — DEBUTRON
- K780348 — EPILATION TYPE DEVICE
- K772322 — DEPILATORY, ELECTRONIC
- K771575 — ELECTRONIC EIPLATOR MODEL NO. 101
- K770186 — ELECTRONIC DEPILATORY MODEL 202
- K770187 — ELECTRONIC DEPILATORY MODEL 303
- K761049 — KENATRON EPILATOR
- K760423 — ELECTROLYSIS MACHINE (PERMATRON)
Data sourced from openFDA. This site is unofficial and independent of the FDA.