The following data is part of a premarket notification filed by Immuno-diagnostic Products, Inc. with the FDA for Cmv Test Kit.
| Device ID | K801963 |
| 510k Number | K801963 |
| Device Name: | CMV TEST KIT |
| Classification | Antigen, Cf (including Cf Control), Cytomegalovirus |
| Applicant | IMMUNO-DIAGNOSTIC PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GQH |
| CFR Regulation Number | 866.3175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-08-19 |
| Decision Date | 1980-10-23 |