The following data is part of a premarket notification filed by Lehigh Consolidated Industries with the FDA for Lci Medical Inc Air/pal.
| Device ID | K841728 |
| 510k Number | K841728 |
| Device Name: | LCI MEDICAL INC AIR/PAL |
| Classification | Device, Patient Transfer, Powered |
| Applicant | LEHIGH CONSOLIDATED INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRZ |
| CFR Regulation Number | 880.6775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-25 |
| Decision Date | 1984-06-05 |