The following data is part of a premarket notification filed by Apollo Enterprise, Ltd. Co. with the FDA for Apollo Mobile Scale.
| Device ID | K905061 |
| 510k Number | K905061 |
| Device Name: | APOLLO MOBILE SCALE |
| Classification | Scale, Patient |
| Applicant | APOLLO ENTERPRISE, LTD. CO. P.O. BOX 218 Somerset, WI 54025 |
| Contact | Adrian Swen |
| Correspondent | Adrian Swen APOLLO ENTERPRISE, LTD. CO. P.O. BOX 218 Somerset, WI 54025 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-11-09 |
| Decision Date | 1991-02-12 |