The following data is part of a premarket notification filed by Tecan U.s., Inc. with the FDA for 4 Channel Dispenser.
| Device ID | K942655 |
| 510k Number | K942655 |
| Device Name: | 4 CHANNEL DISPENSER |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | TECAN U.S., INC. P.O. BOX 13953 Research Triangle Park, NC 27709 |
| Contact | Daniel B Roark |
| Correspondent | Daniel B Roark TECAN U.S., INC. P.O. BOX 13953 Research Triangle Park, NC 27709 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-06 |
| Decision Date | 1994-09-02 |