Electro-Kinetic Manufacturing
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
K770791
Device Name
DEPILATOR, DERMA-I & DERMA-II
Applicant
ELECTRO-KINETIC ENG/MFG
Product Code
KCX
Date Received
05/02/77
Decision Date
01/26/81
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
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Establishment Registration Number:1625431
Establishment Name:
ELECTRO-KINETIC ENT.
3428 GLENVIEW ROAD
GLENVIEW, IL 60025 US
Establishment Operations:
Manufacturer
Owner/Operator Number: 1625431
Owner/Operator:
HONORE M. LARWETH
3428 GLENVIEW ROAD
GLENVIEW, IL 60025 US
Official Correspondent Firm:
ELECTRO-KINETIC ENTERPRISES,NC.
3428 GLENVIEW ROAD
GLENVIEW, IL 60025 US
Establishment Status: Active
Date of Registration Status: 12/08/76
Official Correspondent Phone Number: 312-657-8244
Date Initial Registration Received: 12/08/76
Official Correspondent Name: HONORE LARWETH