The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys Calcheck Ft4.
Device ID | K963164 |
510k Number | K963164 |
Device Name: | ELECSYS CALCHECK FT4 |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
Contact | John D Stevens, Rac |
Correspondent | John D Stevens, Rac BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-08-14 |
Decision Date | 1996-08-27 |
Summary: | summary |