The following data is part of a premarket notification filed by Terumo Medical Corp. with the FDA for Terumo Retractable Needle (rn) Syringe.
| Device ID | K953940 |
| 510k Number | K953940 |
| Device Name: | TERUMO RETRACTABLE NEEDLE (RN) SYRINGE |
| Classification | Syringe, Piston |
| Applicant | TERUMO MEDICAL CORP. 950 Elkton Blvd. Elkton, MD 21921 |
| Contact | Alan B Hershman |
| Correspondent | Alan B Hershman TERUMO MEDICAL CORP. 950 Elkton Blvd. 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 | 1995-08-21 |
| Decision Date | 1996-05-21 |
| Summary: | summary |