The following data is part of a premarket notification filed by Roger Cestac & Assoc. with the FDA for Multitubular Thoracic Air Splints.
| Device ID | K811750 |
| 510k Number | K811750 |
| Device Name: | MULTITUBULAR THORACIC AIR SPLINTS |
| Classification | Orthosis, Thoracic |
| Applicant | ROGER CESTAC & ASSOC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IPT |
| CFR Regulation Number | 890.3490 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-22 |
| Decision Date | 1981-07-20 |