The following data is part of a premarket notification filed by Ch Administration, Inc. with the FDA for Pro-2000 Low Air Loss Therapy Bed.
| Device ID | K926403 |
| 510k Number | K926403 |
| Device Name: | PRO-2000 LOW AIR LOSS THERAPY BED |
| Classification | Mattress, Air Flotation, Alternating Pressure |
| Applicant | CH ADMINISTRATION, INC. P.O. BOX 29923 Dallas, TX 75229 |
| Contact | John A Carbona |
| Correspondent | John A Carbona CH ADMINISTRATION, INC. P.O. BOX 29923 Dallas, TX 75229 |
| Product Code | FNM |
| CFR Regulation Number | 880.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-12-21 |
| Decision Date | 1993-07-30 |