Device Classification Name |
Epilator, High Frequency, Tweezer-Type
|
510(k) Number |
K772322 |
Device Name |
DEPILATORY, ELECTRONIC |
Applicant |
DURA CORP., THE |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
DURA CORP., THE |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.5360
|
Classification Product Code |
|
Date Received | 12/19/1977 |
Decision Date | 01/03/1978 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|