FDA 510(k) Applications Submitted by SAFETY SYRINGES, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K972877 |
08/04/1997 |
ULTRASAFE INJECTION SYSTEM MODEL C200 INJECTOR WITH NEEDLE GUARD |
SAFETY SYRINGES, INC. |
K972878 |
08/04/1997 |
ULTRASAFE INJECTION SYSTEM NEEDLE GUARD, MODELS B50,B100L,B150,B225, AND B300 |
SAFETY SYRINGES, INC. |
K972900 |
08/06/1997 |
ULTRASAFE MODEL T200 INJECTOR |
SAFETY SYRINGES, INC. |
K122558 |
08/22/2012 |
ULTRASAFE PASSIVE NEEDLE GUARD |
SAFETY SYRINGES, INC. |
K123743 |
12/06/2012 |
ULTRASAFE PLUS PASSIVE NEEDLE GUARD |
SAFETY SYRINGES, INC. |
K060743 |
03/20/2006 |
MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE PASSIVE DELIVERY SYSTEM (X-SERIES) |
SAFETY SYRINGES, INC. |
K011369 |
05/04/2001 |
ULTRASAFE PASSIVE X-SERIES, NEEDLE GUARD SYRINGE, PISTON (ACCESSORY) |
SAFETY SYRINGES, INC. |
K042712 |
09/30/2004 |
TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM |
SAFETY SYRINGES, INC. |
K013801 |
11/15/2001 |
ULTRASAFE DENTAL INJECTION SYSTEM |
SAFETY SYRINGES, INC. |
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