The following data is part of a premarket notification filed by Hybritech, Inc. with the FDA for Tandem-e Tsh Calibration Verification Control Set.
| Device ID | K912439 |
| 510k Number | K912439 |
| Device Name: | TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET |
| Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
| Applicant | HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
| Contact | Joanne Martinis |
| Correspondent | Joanne Martinis HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
| Product Code | JJX |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-06-03 |
| Decision Date | 1991-08-28 |