The following data is part of a premarket notification filed by Parke-davis Co. with the FDA for Sponge, Laparotomy Gauze.
| Device ID | K760113 |
| 510k Number | K760113 |
| Device Name: | SPONGE, LAPAROTOMY GAUZE |
| Classification | Gauze/sponge, Internal |
| Applicant | PARKE-DAVIS CO. 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 | 1976-06-24 |
| Decision Date | 1976-07-15 |