The following data is part of a premarket notification filed by Arco Medical Products Co. with the FDA for Arcolith 3022&arcolith 3023 Cardiac Gen..
| Device ID | K800838 |
| 510k Number | K800838 |
| Device Name: | ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN. |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | ARCO MEDICAL PRODUCTS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-04-15 |
| Decision Date | 1980-06-04 |