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SKINCOTE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882567
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/5/1988
Days to Decision
105 days

SKINCOTE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882567
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/5/1988
Days to Decision
105 days