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FDA 510(k), K030853, STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI
FDA 510(k), K030853, STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI
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510(K) Number: K030853
Device Name: STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI
Manufacturer: MARCIA FRIEZE
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 03/18/2003
Decision Date: 03/21/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI
Manufacturer: MARCIA FRIEZE
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 03/18/2003
Decision Date: 03/21/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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