The following data is part of a premarket notification filed by Gelman Instrument Co. with the FDA for Radial Immunodiffusion Kit-comp. 3.
| Device ID | K772073 |
| 510k Number | K772073 |
| Device Name: | RADIAL IMMUNODIFFUSION KIT-COMP. 3 |
| Classification | Complement C4, Antigen, Antiserum, Control |
| Applicant | GELMAN INSTRUMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DBI |
| CFR Regulation Number | 866.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-11-03 |
| Decision Date | 1978-02-03 |