The following data is part of a premarket notification filed by Corda Int'l Holiday, Inc. with the FDA for Lifelift Models One And Two.
| Device ID | K792601 |
| 510k Number | K792601 |
| Device Name: | LIFELIFT MODELS ONE AND TWO |
| Classification | Lift, Patient, Non-ac-powered |
| Applicant | CORDA INT'L HOLIDAY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FSA |
| CFR Regulation Number | 880.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-18 |
| Decision Date | 1979-12-31 |