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FDA 510(k), K991023, STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL
FDA 510(k), K991023, STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL
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510(K) Number: K991023
Device Name: STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL
Manufacturer: LARRY R PILOT
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: 03/29/1999
Date Received: 01/27/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL
Manufacturer: LARRY R PILOT
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: 03/29/1999
Date Received: 01/27/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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