The following data is part of a premarket notification filed by Conco Medical Co. with the FDA for Bandage, E-cotton Elastic.
| Device ID | K760139 |
| 510k Number | K760139 |
| Device Name: | BANDAGE, E-COTTON ELASTIC |
| Classification | Bandage, Elastic |
| Applicant | CONCO MEDICAL CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FQM |
| CFR Regulation Number | 880.5075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-29 |
| Decision Date | 1976-07-19 |