The following data is part of a premarket notification filed by Hemometrix with the FDA for Gentamicin Liquid Control Serum.
| Device ID | K792262 |
| 510k Number | K792262 |
| Device Name: | GENTAMICIN LIQUID CONTROL SERUM |
| Classification | Drug Specific Control Materials |
| Applicant | HEMOMETRIX 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LAS |
| CFR Regulation Number | 862.3280 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-09 |
| Decision Date | 1979-12-18 |