The following data is part of a premarket notification filed by Talley Group Ltd. with the FDA for Talley Micro System/talley Ripplebed.
| Device ID | K914775 |
| 510k Number | K914775 |
| Device Name: | TALLEY MICRO SYSTEM/TALLEY RIPPLEBED |
| Classification | Mattress, Air Flotation, Alternating Pressure |
| Applicant | TALLEY GROUP LTD. 815 TERMINAL RD. Lansing, MI 48906 |
| Contact | Van Dyke |
| Correspondent | Van Dyke TALLEY GROUP LTD. 815 TERMINAL RD. Lansing, MI 48906 |
| Product Code | FNM |
| CFR Regulation Number | 880.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-23 |
| Decision Date | 1992-04-10 |