The following data is part of a premarket notification filed by E.m. Adams with the FDA for Infant Evaluation Carrier.
| Device ID | K831731 |
| 510k Number | K831731 |
| Device Name: | INFANT EVALUATION CARRIER |
| Classification | Stretcher, Hand-carried |
| Applicant | E.M. ADAMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPP |
| CFR Regulation Number | 880.6900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-05-31 |
| Decision Date | 1983-07-18 |