The following data is part of a premarket notification filed by Gull Laboratories, Inc. with the FDA for Cmv Test.
| Device ID | K853137 |
| 510k Number | K853137 |
| Device Name: | CMV TEST |
| Classification | Antiserum, Cf, Cytomegalovirus |
| Applicant | GULL LABORATORIES, INC. 890 EAST 5400 SOUTH Salt Lake City, UT 84107 |
| Contact | Fred W Rachford |
| Correspondent | Fred W Rachford GULL LABORATORIES, INC. 890 EAST 5400 SOUTH Salt Lake City, UT 84107 |
| Product Code | GQI |
| CFR Regulation Number | 866.3175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-26 |
| Decision Date | 1985-11-14 |