FDA 510(k), K941327, CROSSTEX SELF-SEALING STERILIZATION POUCH
FDA 510(k), K941327, CROSSTEX SELF-SEALING STERILIZATION POUCH
Device Name: CROSSTEX SELF-SEALING STERILIZATION POUCH
Manufacturer:
Device Classification Name: Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Regulation Number: 880.6850
Classification Product Code: KCT
Date Received: 03/18/1994
Decision Date: 12/22/1994
Regulation Medical Specialty: General Hospital
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