The following data is part of a premarket notification filed by Professional Medical Products, Inc. with the FDA for Chick/reison Patient Emerg. Trolley.
| Device ID | K834478 |
| 510k Number | K834478 |
| Device Name: | CHICK/REISON PATIENT EMERG. TROLLEY |
| Classification | Table, Radiologic |
| Applicant | PROFESSIONAL MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KXJ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-20 |
| Decision Date | 1984-02-21 |