The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys Myoglobin Stat Assay.
Device ID | K983176 |
510k Number | K983176 |
Device Name: | ELECSYS MYOGLOBIN STAT ASSAY |
Classification | Myoglobin, Antigen, Antiserum, Control |
Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
Contact | Priscilla A Hamill |
Correspondent | Priscilla A Hamill BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
Product Code | DDR |
CFR Regulation Number | 866.5680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-10 |
Decision Date | 1998-09-24 |
Summary: | summary |