The following data is part of a premarket notification filed by Dutchland Laboratories, Inc. with the FDA for Rpmi 1640 Medium.
| Device ID | K810767 |
| 510k Number | K810767 |
| Device Name: | RPMI 1640 MEDIUM |
| Classification | Media And Components, Synthetic Cell And Tissue Culture |
| Applicant | DUTCHLAND LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KIT |
| CFR Regulation Number | 864.2220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-23 |
| Decision Date | 1981-05-08 |