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HIGH FREQUENCY EPILATOR CB-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823674
510(k) Type
Traditional
Applicant
R. A. FISCHER CO. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1983
Days to Decision
38 days

HIGH FREQUENCY EPILATOR CB-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823674
510(k) Type
Traditional
Applicant
R. A. FISCHER CO. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1983
Days to Decision
38 days