INVALIFT
Device, Patient Transfer, Powered
AMERICAN INVALIFT CORP.
The following data is part of a premarket notification filed by American Invalift Corp. with the FDA for Invalift.
Pre-market Notification Details
| Device ID | K910830 |
| 510k Number | K910830 |
| Device Name: | INVALIFT |
| Classification | Device, Patient Transfer, Powered |
| Applicant | AMERICAN INVALIFT CORP. 285 TARRYTOWN RD. White Plains, NY 10607 |
| Contact | Therese Rubino |
| Correspondent | Therese Rubino AMERICAN INVALIFT CORP. 285 TARRYTOWN RD. White Plains, NY 10607 |
| Product Code | FRZ |
| CFR Regulation Number | 880.6775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-27 |
| Decision Date | 1992-06-09 |
Trademark Results [INVALIFT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INVALIFT 81038154 1038154 Dead/Cancelled |
Loos; August W. 0000-00-00 |
 INVALIFT 73059523 1054265 Dead/Cancelled |
Invalift, Inc. 1975-08-04 |
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