The following data is part of a premarket notification filed by Parke-davis Co. with the FDA for Orthopedic Tubular Stockinette.
| Device ID | K760817 |
| 510k Number | K760817 |
| Device Name: | ORTHOPEDIC TUBULAR STOCKINETTE |
| Classification | Stocking, Elastic |
| Applicant | PARKE-DAVIS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ILG |
| CFR Regulation Number | 890.3475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-10-12 |
| Decision Date | 1976-10-20 |