The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys T4 Assay.
Device ID | K961490 |
510k Number | K961490 |
Device Name: | ELECSYS T4 ASSAY |
Classification | Radioimmunoassay, Total Thyroxine |
Applicant | BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. P.O. BOX 4117 Concord, CA 94524 -4117 |
Contact | Mary Koning |
Correspondent | Mary Koning BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. P.O. BOX 4117 Concord, CA 94524 -4117 |
Product Code | CDX |
CFR Regulation Number | 862.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-04-18 |
Decision Date | 1996-06-13 |
Summary: | summary |