The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Sam Ls.
| Device ID | K913095 |
| 510k Number | K913095 |
| Device Name: | SAM LS |
| Classification | Nebulizer (direct Patient Interface) |
| Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Contact | Frank Ferguson |
| Correspondent | Frank Ferguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Product Code | CAF |
| CFR Regulation Number | 868.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-07-12 |
| Decision Date | 1992-12-03 |