The following data is part of a premarket notification filed by Micromedics, Inc. with the FDA for Cody Sacculotomy Tack.
| Device ID | K832068 |
| 510k Number | K832068 |
| Device Name: | CODY SACCULOTOMY TACK |
| Classification | Tack, Sacculotomy (cody Tack) |
| Applicant | MICROMEDICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ESX |
| CFR Regulation Number | 874.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-27 |
| Decision Date | 1983-10-19 |