The following data is part of a premarket notification filed by Biological Corp. Of America with the FDA for Elution Solution.
| Device ID | K812565 |
| 510k Number | K812565 |
| Device Name: | ELUTION SOLUTION |
| Classification | Media, Potentiating For In Vitro Diagnostic Use |
| Applicant | BIOLOGICAL CORP. OF AMERICA 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KSG |
| CFR Regulation Number | 864.9600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-09-09 |
| Decision Date | 1981-10-23 |