The following data is part of a premarket notification filed by Roche Diagnostics with the FDA for Elecsys Cea Calcheck 5.
Device ID | K101856 |
510k Number | K101856 |
Device Name: | ELECSYS CEA CALCHECK 5 |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | Roche Diagnostics 9115 HAGUE RD Indianapolis, IN 46250 |
Contact | Jason Fisher |
Correspondent | Jason Fisher Roche Diagnostics 9115 HAGUE RD Indianapolis, IN 46250 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-07-01 |
Decision Date | 2010-10-05 |
Summary: | summary |