Last synced on 24 March 2023 at 11:04 pm

DEPILATOR, DERMA-I & DERMA-II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770791
510(k) Type
Traditional
Applicant
ELECTRO-KINETIC ENG/MFG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1981
Days to Decision
1365 days

DEPILATOR, DERMA-I & DERMA-II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770791
510(k) Type
Traditional
Applicant
ELECTRO-KINETIC ENG/MFG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1981
Days to Decision
1365 days