The following data is part of a premarket notification filed by Ulster Scientific, Inc. with the FDA for Epc Electronic Pipetting System.
| Device ID | K902592 |
| 510k Number | K902592 |
| Device Name: | EPC ELECTRONIC PIPETTING SYSTEM |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | ULSTER SCIENTIFIC, INC. P.O. BOX 902 Highland, NY 12528 |
| Contact | Richard Cunningham |
| Correspondent | Richard Cunningham ULSTER SCIENTIFIC, INC. P.O. BOX 902 Highland, NY 12528 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-12 |
| Decision Date | 1990-07-19 |