The following data is part of a premarket notification filed by Ventrex Laboratories, Inc. with the FDA for Centria Prolactin Test Set.
| Device ID | K813572 |
| 510k Number | K813572 |
| Device Name: | CENTRIA PROLACTIN TEST SET |
| Classification | Radioimmunoassay, Prolactin (lactogen) |
| Applicant | VENTREX LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CFT |
| CFR Regulation Number | 862.1625 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-22 |
| Decision Date | 1982-03-26 |