The following data is part of a premarket notification filed by S & W Medico Teknik with the FDA for Type 9240 Ecg/resp Syst Athena (adult & Pediatic).
| Device ID | K884120 |
| 510k Number | K884120 |
| Device Name: | TYPE 9240 ECG/RESP SYST ATHENA (ADULT & PEDIATIC) |
| Classification | Monitor, Breathing Frequency |
| 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 | BZQ |
| CFR Regulation Number | 868.2375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-30 |
| Decision Date | 1990-07-17 |