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FDA 510(k), K060743, MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)
FDA 510(k), K060743, MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)
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510(K) Number: K060743
Device Name: MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)
Manufacturer: SAFETY SYRINGES, INC.
Device Classification Name: syringe, antistick
Regulation Number: 880.5860
Classification Product Code: MEG
Date Received: 03/20/2006
Decision Date: 04/28/2006
Regulation Medical Specialty: General Hospital
Device Name: MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES)
Manufacturer: SAFETY SYRINGES, INC.
Device Classification Name: syringe, antistick
Regulation Number: 880.5860
Classification Product Code: MEG
Date Received: 03/20/2006
Decision Date: 04/28/2006
Regulation Medical Specialty: General Hospital
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