The following data is part of a premarket notification filed by Inova Diagnostics, Inc. with the FDA for Quanta Lite B2gpi Igm.
Device ID | K973014 |
510k Number | K973014 |
Device Name: | QUANTA LITE B2GPI IGM |
Classification | System,test,antibodies,b2 - Glycoprotein I (b2 - Gpi) |
Applicant | INOVA DIAGNOSTICS, INC. 10451 ROSELLE ST. San Diego, CA 92121 |
Contact | Brys C Myers |
Correspondent | Brys C Myers INOVA DIAGNOSTICS, INC. 10451 ROSELLE ST. San Diego, CA 92121 |
Product Code | MSV |
CFR Regulation Number | 866.5660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-08-13 |
Decision Date | 1997-10-20 |