The following data is part of a premarket notification filed by Carwild Corp. with the FDA for Neurological Sponges (patties).
| Device ID | K791871 |
| 510k Number | K791871 |
| Device Name: | NEUROLOGICAL SPONGES (PATTIES) |
| Classification | Gauze/sponge, Internal |
| Applicant | CARWILD CORP. 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 | 1979-09-21 |
| Decision Date | 1979-11-05 |