The following data is part of a premarket notification filed by Dennison Manufacturing Co. with the FDA for Sterile Tubular Unbleached Stockinette.
| Device ID | K760750 |
| 510k Number | K760750 |
| Device Name: | STERILE TUBULAR UNBLEACHED STOCKINETTE |
| Classification | Conversion To Ferric Hydroxymates (colorimetric), Fatty Acids |
| Applicant | DENNISON MANUFACTURING CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JLG |
| CFR Regulation Number | 862.1290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-10-01 |
| Decision Date | 1976-10-08 |