The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Lifepak 7d.
| Device ID | K840047 |
| 510k Number | K840047 |
| Device Name: | LIFEPAK 7D |
| Classification | Pacemaker, Cardiac, External Transcutaneous (non-invasive) |
| Applicant | PHYSIO-CONTROL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRO |
| CFR Regulation Number | 870.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-06 |
| Decision Date | 1984-02-04 |