The following data is part of a premarket notification filed by Seamed Corp. with the FDA for Sea Med Model 880.
| Device ID | K823048 |
| 510k Number | K823048 |
| Device Name: | SEA MED MODEL 880 |
| Classification | Pulse-generator, Pacemaker, External |
| Applicant | SEAMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTE |
| CFR Regulation Number | 870.3600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-15 |
| Decision Date | 1982-12-15 |