The following data is part of a premarket notification filed by Acme Medical Scale Co. with the FDA for Scale, Acme Digital Bedside.
| Device ID | K781832 |
| 510k Number | K781832 |
| Device Name: | SCALE, ACME DIGITAL BEDSIDE |
| Classification | Scale, Patient |
| Applicant | ACME MEDICAL SCALE CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-30 |
| Decision Date | 1978-12-07 |