Last synced on 14 November 2025 at 11:06 pm

EPILATOR

Page Type
Cleared 510(K)
510(k) Number
K952117
510(k) Type
Traditional
Applicant
BURKE NEUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1995
Days to Decision
167 days
Submission Type
Statement

EPILATOR

Page Type
Cleared 510(K)
510(k) Number
K952117
510(k) Type
Traditional
Applicant
BURKE NEUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1995
Days to Decision
167 days
Submission Type
Statement