The following data is part of a premarket notification filed by Dutton-lainson Co. with the FDA for Sanitas Patient Scale.
| Device ID | K930626 |
| 510k Number | K930626 |
| Device Name: | SANITAS PATIENT SCALE |
| Classification | Scale, Patient |
| Applicant | DUTTON-LAINSON CO. 451 WEST SECOND ST. Hastings, NE 68902 |
| Contact | Ron Haase |
| Correspondent | Ron Haase DUTTON-LAINSON CO. 451 WEST SECOND ST. Hastings, NE 68902 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-08 |
| Decision Date | 1993-08-06 |