The following data is part of a premarket notification filed by Gemini, Inc. with the FDA for Gemeni Quick-mb Separation Kit.
| Device ID | K810534 |
| 510k Number | K810534 |
| Device Name: | GEMENI QUICK-MB SEPARATION KIT |
| Classification | Chromatographic Separation, Cpk Isoenzymes |
| Applicant | GEMINI, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JHT |
| CFR Regulation Number | 862.1215 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-26 |
| Decision Date | 1981-03-11 |