The following data is part of a premarket notification filed by Bd with the FDA for Bd Spring Based Syringe.
| Device ID | K011103 |
| 510k Number | K011103 |
| Device Name: | BD SPRING BASED SYRINGE |
| Classification | Syringe, Antistick |
| Applicant | BD 1 BECTON DR. MC 226 Franklin Lakes, NJ 07417 |
| Contact | Greg W Morgan |
| Correspondent | Greg W Morgan BD 1 BECTON DR. MC 226 Franklin Lakes, NJ 07417 |
| Product Code | MEG |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-04-11 |
| Decision Date | 2001-06-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50382903058339 | K011103 | 000 |
| 50382903052702 | K011103 | 000 |
| 50382903052719 | K011103 | 000 |
| 50382903052726 | K011103 | 000 |
| 50382903052733 | K011103 | 000 |
| 50382903052740 | K011103 | 000 |
| 50382903052757 | K011103 | 000 |
| 50382903052832 | K011103 | 000 |
| 50382903053105 | K011103 | 000 |
| 50382903053112 | K011103 | 000 |
| 50382903053129 | K011103 | 000 |
| 50382903053136 | K011103 | 000 |
| 50382903052696 | K011103 | 000 |