The following data is part of a premarket notification filed by Hybritech, Inc. with the FDA for Tandem-e Ferritin Calibration Verification Conrol.
Device ID | K921252 |
510k Number | K921252 |
Device Name: | TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | HYBRITECH, INC. P.O. BOX 269006 San Diego, CA 92196 |
Contact | Joanne Martinis |
Correspondent | Joanne Martinis HYBRITECH, INC. P.O. BOX 269006 San Diego, CA 92196 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-03-16 |
Decision Date | 1992-07-17 |