The following data is part of a premarket notification filed by Diagnostic Products Corp. with the FDA for Winmax Software Systems.
| Device ID | K965103 |
| 510k Number | K965103 |
| Device Name: | WINMAX SOFTWARE SYSTEMS |
| Classification | Analyzer, Chemistry, Micro, For Clinical Use |
| Applicant | DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Contact | Edward M Levine |
| Correspondent | Edward M Levine DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Product Code | JJF |
| Subsequent Product Code | DGC |
| Subsequent Product Code | DHB |
| CFR Regulation Number | 862.2170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-12-20 |
| Decision Date | 1997-05-09 |
| Summary: | summary |