Dura Corporation
Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing.
Contact information
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Available devices
Epilator name | FDA 510(k) | Cleared |
NotesDevice Classification Name
EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE
Regulation Number
878.5360
510(k) Number
K772322
Device Name
DEPILATORY, ELECTRONIC
Applicant
DURA CORP., THE
Product Code
KCX
Date Received
12/19/77
Decision Date
01/03/78
Decision
Substantially Equivalent
Classification Advisory Committee
General & Plastic Surgery
Review Advisory Committee
General & Plastic Surgery
Statement/Summary/Purged Indicator
Purged, no summary or statement
Type
Traditional