The following data is part of a premarket notification filed by Roche Diagnostics with the FDA for Elecsys Pth Calcheck 5.
Device ID | K103162 |
510k Number | K103162 |
Device Name: | ELECSYS PTH CALCHECK 5 |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | Roche Diagnostics 9115 HAGUE ROAD Indianapolis, IN 46250 -0416 |
Contact | Kelly French |
Correspondent | Kelly French Roche Diagnostics 9115 HAGUE ROAD Indianapolis, IN 46250 -0416 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-10-27 |
Decision Date | 2010-11-18 |
Summary: | summary |