The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys Calcheck Folate.
Device ID | K974384 |
510k Number | K974384 |
Device Name: | ELECSYS CALCHECK FOLATE |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | BOEHRINGER MANNHEIM CORP. 4300 HACIENDA DR. Pleasanton, CA 94588 -2722 |
Contact | Patricia M Klimley |
Correspondent | Patricia M Klimley BOEHRINGER MANNHEIM CORP. 4300 HACIENDA DR. Pleasanton, CA 94588 -2722 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-11-21 |
Decision Date | 1997-12-08 |
Summary: | summary |