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FDA 510(k), K090068, STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
FDA 510(k), K090068, STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
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510(K) Number: K090068
Device Name: STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
Manufacturer: TANIA LUPU
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 01/09/2009
Decision Date: 02/24/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
Manufacturer: TANIA LUPU
Device Classification Name: Wrap, Sterilization
Regulation Number: FRG
Classification Product Code: KXA
Date Received: 01/09/2009
Decision Date: 02/24/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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