The following data is part of a premarket notification filed by Ulti-med Intl., Inc. with the FDA for Gauze & Lab Sponges Sterile & Non.
| Device ID | K842572 |
| 510k Number | K842572 |
| Device Name: | GAUZE & LAB SPONGES STERILE & NON |
| Classification | Gauze/sponge, Internal, X-ray Detectable |
| Applicant | ULTI-MED INTL., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GDY |
| CFR Regulation Number | 878.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-07-03 |
| Decision Date | 1984-08-15 |