The following data is part of a premarket notification filed by Hemagen Diagnostics, Inc. with the FDA for Hemagen Crp 150 Kit (eia Method).
| Device ID | K960324 |
| 510k Number | K960324 |
| Device Name: | HEMAGEN CRP 150 KIT (EIA METHOD) |
| Classification | C-reactive Protein, Antigen, Antiserum, And Control |
| Applicant | HEMAGEN DIAGNOSTICS, INC. 34-40 BEAR HILL RD. Waltlham, MA 02154 |
| Contact | Joseph M Califano |
| Correspondent | Joseph M Califano HEMAGEN DIAGNOSTICS, INC. 34-40 BEAR HILL RD. Waltlham, MA 02154 |
| Product Code | DCK |
| CFR Regulation Number | 866.5270 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-23 |
| Decision Date | 1996-03-12 |
| Summary: | summary |