The following data is part of a premarket notification filed by Medical Technomics, Ltd. with the FDA for Eppendorf Diluter.
| Device ID | K844798 |
| 510k Number | K844798 |
| Device Name: | EPPENDORF DILUTER |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | MEDICAL TECHNOMICS, LTD. 770-D NORTH CHURCH RD. Elmhurst, IL 60126 |
| Contact | Dennis A Aldred |
| Correspondent | Dennis A Aldred MEDICAL TECHNOMICS, LTD. 770-D NORTH CHURCH RD. Elmhurst, IL 60126 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-12-11 |
| Decision Date | 1985-01-07 |