The following data is part of a premarket notification filed by Bd with the FDA for Interlink Threaded Lock Cannula.
| Device ID | K011858 |
| 510k Number | K011858 |
| Device Name: | INTERLINK THREADED LOCK CANNULA |
| Classification | Set, Administration, Intravascular |
| Applicant | BD 1 BECTON DR. MC 226 Franklin Lakes, NJ 07417 |
| Contact | Gregory W Morgan |
| Correspondent | Gregory W Morgan BD 1 BECTON DR. MC 226 Franklin Lakes, NJ 07417 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-06-14 |
| Decision Date | 2001-06-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50382903033695 | K011858 | 000 |
| 30382903033790 | K011858 | 000 |