The following data is part of a premarket notification filed by Nanosphere, Inc with the FDA for Verigene Respiratory Virus Nucleic Acid Test.
Device ID | K083088 |
510k Number | K083088 |
Device Name: | VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST |
Classification | Respiratory Virus Panel Nucleic Acid Assay System |
Applicant | NANOSPHERE, INC 4088 COMMERCIAL AVENUE Northbrook, IL 60062 |
Contact | Gregory W Shipp |
Correspondent | Gregory W Shipp NANOSPHERE, INC 4088 COMMERCIAL AVENUE Northbrook, IL 60062 |
Product Code | OCC |
CFR Regulation Number | 866.3980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-10-16 |
Decision Date | 2009-05-01 |
Summary: | summary |