The following data is part of a premarket notification filed by Kinetic Concepts, Inc. with the FDA for Fluidair.
| Device ID | K881917 |
| 510k Number | K881917 |
| Device Name: | FLUIDAIR |
| Classification | Bed, Air Fluidized |
| Applicant | KINETIC CONCEPTS, INC. 3440 EAST HOUSTON ST. San Antonio, TX 78219 |
| Contact | Robert A Wehrmeyer |
| Correspondent | Robert A Wehrmeyer KINETIC CONCEPTS, INC. 3440 EAST HOUSTON ST. San Antonio, TX 78219 |
| Product Code | INX |
| CFR Regulation Number | 890.5160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-09 |
| Decision Date | 1988-11-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FLUIDAIR 76533020 2957676 Live/Registered |
HUNTLEIGH TECHNOLOGY LTD. 2003-07-17 |
![]() FLUIDAIR 72395395 0959295 Dead/Expired |
FLUIDAIR COMPRESSORS LIMITED 1971-06-21 |