The following data is part of a premarket notification filed by Dutchland Laboratories, Inc. with the FDA for L-15 Powdered Medium.
| Device ID | K820917 |
| 510k Number | K820917 |
| Device Name: | L-15 POWDERED MEDIUM |
| Classification | Media And Components, Synthetic Cell And Tissue Culture |
| Applicant | DUTCHLAND LABORATORIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KIT |
| CFR Regulation Number | 864.2220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-01 |
| Decision Date | 1982-04-21 |