The following data is part of a premarket notification filed by Ascep, Inc. with the FDA for Catheter Care Kit Reorder 7940&7941.
| Device ID | K791888 |
| 510k Number | K791888 |
| Device Name: | CATHETER CARE KIT REORDER 7940&7941 |
| Classification | Gauze/sponge, Internal |
| Applicant | ASCEP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EFQ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-09-11 |
| Decision Date | 1979-10-17 |