The following data is part of a premarket notification filed by Top Surgical Manufacturers Co. with the FDA for Winged Infusion Set.
| Device ID | K832622 |
| 510k Number | K832622 |
| Device Name: | WINGED INFUSION SET |
| Classification | Set, Administration, Intravascular |
| Applicant | TOP SURGICAL MANUFACTURERS CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-04 |
| Decision Date | 1983-10-14 |