The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Stille Automatic Tourniquet.
| Device ID | K925033 |
| 510k Number | K925033 |
| Device Name: | STILLE AUTOMATIC TOURNIQUET |
| Classification | Tourniquet, Pneumatic |
| Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Contact | Frank Gerguson |
| Correspondent | Frank Gerguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Product Code | KCY |
| CFR Regulation Number | 878.5910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-05 |
| Decision Date | 1993-02-01 |