The following data is part of a premarket notification filed by Siemens Healthcare Diagnostics Inc. with the FDA for Immulite: 2000 Free T4 Calibration Verification Material, 2000 Igf-i Calibration Verification Material, 2000 Prolactin C.
Device ID | K140818 |
510k Number | K140818 |
Device Name: | IMMULITE: 2000 FREE T4 CALIBRATION VERIFICATION MATERIAL, 2000 IGF-I CALIBRATION VERIFICATION MATERIAL, 2000 PROLACTIN C |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | Siemens Healthcare Diagnostics Inc. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Contact | Ernest Joseph |
Correspondent | Ernest Joseph Siemens Healthcare Diagnostics Inc. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-04-01 |
Decision Date | 2014-05-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00630414979427 | K140818 | 000 |
00630414973647 | K140818 | 000 |
00630414971247 | K140818 | 000 |