The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Lifepak 5 Cardioscope-recorder Module.
| Device ID | K760676 |
| 510k Number | K760676 |
| Device Name: | LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE |
| Classification | Recorder, Paper Chart |
| Applicant | PHYSIO-CONTROL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSF |
| CFR Regulation Number | 870.2810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-20 |
| Decision Date | 1976-10-13 |