The following data is part of a premarket notification filed by Sa Scientific, Inc. with the FDA for Sas Flualert A&b, Sas Influenza A Test.
Device ID | K100227 |
510k Number | K100227 |
Device Name: | SAS FLUALERT A&B, SAS INFLUENZA A TEST |
Classification | Devices Detecting Influenza A, B, And C Virus Antigens |
Applicant | SA SCIENTIFIC, INC. 4919 GOLDEN QUAIL San Antonio, TX 78240 |
Contact | Robbi Perry |
Correspondent | Robbi Perry SA SCIENTIFIC, INC. 4919 GOLDEN QUAIL San Antonio, TX 78240 |
Product Code | PSZ |
CFR Regulation Number | 866.3328 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-01-26 |
Decision Date | 2010-02-23 |
Summary: | summary |