The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Srd-2.
| Device ID | K781646 |
| 510k Number | K781646 |
| Device Name: | SRD-2 |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | DYNATECH LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-09-25 |
| Decision Date | 1978-10-27 |