The following data is part of a premarket notification filed by Immucor, Inc. with the FDA for Potentiating Media For In Vitro Diagnostic Use.
| Device ID | BK920033 |
| 510k Number | BK920033 |
| Device Name: | Potentiating Media For In Vitro Diagnostic Use |
| Classification | Media, Potentiating For In Vitro Diagnostic Use |
| Applicant | Immucor, Inc. 3130 Gateway Drive p.o. Box 5625 Norcross, GA 30091 |
| Product Code | KSG |
| CFR Regulation Number | 864.9600 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-10 |
| Decision Date | 1993-09-21 |