The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Emergency Cart.
| Device ID | K772320 |
| 510k Number | K772320 |
| Device Name: | EMERGENCY CART |
| Classification | Cart, Emergency, Cardiopulmonary (excluding Equipment) |
| Applicant | PHYSIO-CONTROL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZN |
| CFR Regulation Number | 868.6175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-19 |
| Decision Date | 1978-01-03 |