The following data is part of a premarket notification filed by Safety Syringes, Inc. with the FDA for Ultrasafe Model T200 Injector.
| Device ID | K972900 |
| 510k Number | K972900 |
| Device Name: | ULTRASAFE MODEL T200 INJECTOR |
| Classification | Syringe, Piston |
| Applicant | SAFETY SYRINGES, INC. 250 WEST COLORADO BLVD., #101 Arcadia, CA 91007 |
| Contact | Anthony Perez |
| Correspondent | Anthony Perez SAFETY SYRINGES, INC. 250 WEST COLORADO BLVD., #101 Arcadia, CA 91007 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-06 |
| Decision Date | 1998-02-26 |
| Summary: | summary |