The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Tina-quant Ferritin Assay.
Device ID | K964282 |
510k Number | K964282 |
Device Name: | TINA-QUANT FERRITIN ASSAY |
Classification | Radioimmunoassay (two-site Solid Phase), Ferritin |
Applicant | BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
Contact | Yvette Lloyd |
Correspondent | Yvette Lloyd BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
Product Code | JMG |
CFR Regulation Number | 866.5340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-10-28 |
Decision Date | 1997-07-30 |
Summary: | summary |