The following data is part of a premarket notification filed by Medpro, Inc. with the FDA for Medpro Flotation System.
| Device ID | K771824 |
| 510k Number | K771824 |
| Device Name: | MEDPRO FLOTATION SYSTEM |
| Classification | Mattress, Flotation Therapy, Non-powered |
| Applicant | MEDPRO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IKY |
| CFR Regulation Number | 880.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-09-27 |
| Decision Date | 1977-10-19 |