The following data is part of a premarket notification filed by S & W Medico Teknik with the FDA for Type 9040 System Athena.
| Device ID | K884116 |
| 510k Number | K884116 |
| Device Name: | TYPE 9040 SYSTEM ATHENA |
| Classification | Electrocardiograph |
| Applicant | S & W MEDICO TEKNIK HERSTEDVANG 8 DK-2620 ALBERTSLUND Denmark, DK |
| Contact | Lisbeth Isbrandt |
| Correspondent | Lisbeth Isbrandt S & W MEDICO TEKNIK HERSTEDVANG 8 DK-2620 ALBERTSLUND Denmark, DK |
| Product Code | DPS |
| CFR Regulation Number | 870.2340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-30 |
| Decision Date | 1989-04-26 |