The following data is part of a premarket notification filed by Huntleigh Technology, Inc. with the FDA for Huntleigh Dynamic Flotation System.
| Device ID | K890012 |
| 510k Number | K890012 |
| Device Name: | HUNTLEIGH DYNAMIC FLOTATION SYSTEM |
| Classification | Mattress, Air Flotation, Alternating Pressure |
| Applicant | HUNTLEIGH TECHNOLOGY, INC. 227 ROUTE 33 EAST Manalapan, NJ 07726 |
| Contact | James Britton |
| Correspondent | James Britton HUNTLEIGH TECHNOLOGY, INC. 227 ROUTE 33 EAST Manalapan, NJ 07726 |
| Product Code | FNM |
| CFR Regulation Number | 880.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-03 |
| Decision Date | 1989-03-29 |