The following data is part of a premarket notification filed by Corpak Co. with the FDA for Enternal Solution Admin. Set.
| Device ID | K821036 |
| 510k Number | K821036 |
| Device Name: | ENTERNAL SOLUTION ADMIN. SET |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | CORPAK CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-13 |
| Decision Date | 1982-04-26 |