Baxter Healthcare Corp · Class II · Cleared Jun 26, 1996
| K-number | K961495 |
| Device name | HUBER NEEDLE EXTENSION SET WITH STANDARD Y-INJECTION SITE, INTERLINK Y-INJECTION SITE, INTERLINK T-INJECTION SITE |
| Applicant | Baxter Healthcare Corp |
| Product code | FPA |
| Device class | Class II |
| Decision date | Jun 26, 1996 |
| 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