Baxter Healthcare Corp · Class II · Cleared Nov 27, 1991
| K-number | K914048 |
| Device name | NEEDLE*LOCK(TM) WITH INTERLINK(TM) INJECTION SITE |
| Applicant | Baxter Healthcare Corp |
| Product code | FPA |
| Device class | Class II |
| Decision date | Nov 27, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 880.5440 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov