Last synced on 25 January 2026 at 3:41 am

ANGIOMED SKIN FASCIA KNIFE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K855104
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1986
Days to Decision
32 days

ANGIOMED SKIN FASCIA KNIFE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K855104
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1986
Days to Decision
32 days