The following data is part of a premarket notification filed by Bd Becton Dickinson Vacutainer Systems Preanalytic with the FDA for Becton Dickinson Safety-lok Syringe.
| Device ID | K924072 |
| 510k Number | K924072 |
| Device Name: | BECTON DICKINSON SAFETY-LOK SYRINGE |
| Classification | Syringe, Piston |
| Applicant | BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DR. Franklin Lakes, NJ 07417 -1880 |
| Contact | Marcia C Leatham |
| Correspondent | Marcia C Leatham BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DR. Franklin Lakes, NJ 07417 -1880 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-12 |
| Decision Date | 1992-12-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10889942303380 | K924072 | 000 |
| 10888277006812 | K924072 | 000 |
| 10884389580523 | K924072 | 000 |