The following data is part of a premarket notification filed by Terumo Corp. with the FDA for Terumo Allergy Syringe.
| Device ID | K980796 |
| 510k Number | K980796 |
| Device Name: | TERUMO ALLERGY SYRINGE |
| Classification | Syringe, Piston |
| Applicant | TERUMO CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
| Contact | Kristine Wagner |
| Correspondent | Kristine Wagner TERUMO CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-03-02 |
| Decision Date | 1998-04-02 |
| Summary: | summary |