The following data is part of a premarket notification filed by Tosoh Medics, Inc. with the FDA for St Aia-pack Testosterone Assay.
| Device ID | K023091 |
| 510k Number | K023091 |
| Device Name: | ST AIA-PACK TESTOSTERONE ASSAY |
| Classification | Radioimmunoassay, Testosterones And Dihydrotestosterone |
| Applicant | TOSOH MEDICS, INC. 347 OYSTER POINT BLVD., SUITE 201 San Francisco, CA 94080 |
| Contact | Lois Nakayama |
| Correspondent | Lois Nakayama TOSOH MEDICS, INC. 347 OYSTER POINT BLVD., SUITE 201 San Francisco, CA 94080 |
| Product Code | CDZ |
| CFR Regulation Number | 862.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-09-17 |
| Decision Date | 2002-12-17 |
| Summary: | summary |