The following data is part of a premarket notification filed by Sage Products, Inc. with the FDA for Stp System - Saf.
| Device ID | K964026 |
| 510k Number | K964026 |
| Device Name: | STP SYSTEM - SAF |
| Classification | Device, Specimen Collection |
| Applicant | SAGE PRODUCTS, INC. 815 TEK DR. Crystal Lake, IL 60014 -8172 |
| Contact | Karen Pinto |
| Correspondent | Karen Pinto SAGE PRODUCTS, INC. 815 TEK DR. Crystal Lake, IL 60014 -8172 |
| Product Code | LIO |
| CFR Regulation Number | 866.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-10-07 |
| Decision Date | 1996-11-07 |
| Summary: | summary |