The following data is part of a premarket notification filed by Nanosphere, Inc. with the FDA for Verigene Respiratory Virus Nucleic Acid Test +(rvnat+).
Device ID | K103209 |
510k Number | K103209 |
Device Name: | VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST +(RVNAT+) |
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 | 2010-11-01 |
Decision Date | 2011-01-10 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00857573006294 | K103209 | 000 |
00857573006232 | K103209 | 000 |
00857573006133 | K103209 | 000 |