The following data is part of a premarket notification filed by Supportech, Inc. with the FDA for Prenatal Support Pillow.
| Device ID | K810035 |
| 510k Number | K810035 |
| Device Name: | PRENATAL SUPPORT PILLOW |
| Classification | Support, Patient Position |
| Applicant | SUPPORTECH, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CCX |
| CFR Regulation Number | 868.6820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-01-09 |
| Decision Date | 1981-01-23 |