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AC-22 AUTOCLAVE TAPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831722
510(k) Type
Traditional
Applicant
ARMAK TAPE DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1983
Days to Decision
36 days

AC-22 AUTOCLAVE TAPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831722
510(k) Type
Traditional
Applicant
ARMAK TAPE DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1983
Days to Decision
36 days