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STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001649
510(k) Type
Abbreviated
Applicant
STERITEC PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
24 days
Submission Type
Statement

STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001649
510(k) Type
Abbreviated
Applicant
STERITEC PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
24 days
Submission Type
Statement