The following data is part of a premarket notification filed by Baxter Healthcare Corp. with the FDA for Safesite Injection Site And Blunt Cannula.
| Device ID | K883638 |
| 510k Number | K883638 |
| Device Name: | SAFESITE INJECTION SITE AND BLUNT CANNULA |
| Classification | Set, Administration, Intravascular |
| Applicant | BAXTER HEALTHCARE CORP. ROUTE 120 AND WILSON RD. Round Lake, IL 60073 |
| Contact | Dennis Ocwieja |
| Correspondent | Dennis Ocwieja BAXTER HEALTHCARE CORP. ROUTE 120 AND WILSON RD. Round Lake, IL 60073 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-25 |
| Decision Date | 1988-09-23 |