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FDA 510(k), K974638, STERITITE SEALED CONTAINERS MODEL SCO4Q
FDA 510(k), K974638, STERITITE SEALED CONTAINERS MODEL SCO4Q
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510(K) Number: K974638
Device Name: STERITITE SEALED CONTAINERS MODEL SCO4Q
Manufacturer: LARRY R PILOT
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 10/10/1997
Decision Date: 12/18/1997
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERITITE SEALED CONTAINERS MODEL SCO4Q
Manufacturer: LARRY R PILOT
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 10/10/1997
Decision Date: 12/18/1997
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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