The following data is part of a premarket notification filed by Befour, Inc. with the FDA for Hamilton Pediatrics Scale.
| Device ID | K833754 |
| 510k Number | K833754 |
| Device Name: | HAMILTON PEDIATRICS SCALE |
| Classification | Scale, Patient |
| Applicant | BEFOUR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-26 |
| Decision Date | 1984-01-11 |