Electronic Depilatory Co.
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 |
Notes
Device Classification Name
EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE
Regulation Number
878.5360
510(k) Number
K771575
Device Name
ELECTRONIC EIPLATOR MODEL NO. 101
Applicant
ELECTRONIC DEPILATORY, INC.
Product Code
KCX
Date Received
08/16/77
Decision Date
09/06/77
Decision
Substantially Equivalent
Classification Advisory Committee
General & Plastic Surgery
Review Advisory Committee
Physical Medicine
Statement/Summary/Purged Indicator
Purged, no summary or statement
Type
Traditional
Device Classification Name
EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE
Regulation Number
878.5360
510(k) Number
K770186
Device Name
ELECTRONIC DEPILATORY MODEL 202
Applicant
ELECTRONIC DEPILATORY, INC.
Product Code
KCX
Date Received
01/27/77
Decision Date
02/23/77
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
Device Classification Name
EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE
Regulation Number
878.5360
510(k) Number
K770187
Device Name
ELECTRONIC DEPILATORY MODEL 303
Applicant
ELECTRONIC DEPILATORY, INC.
Product Code
KCX
Date Received
01/27/77
Decision Date
02/23/77
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