The following data is part of a premarket notification filed by Alere Scarborough, Inc D/b/a Binax, Inc. with the FDA for Alere Influenza A & B Test.
| Device ID | K133637 |
| 510k Number | K133637 |
| Device Name: | ALERE INFLUENZA A & B TEST |
| Classification | Devices Detecting Influenza A, B, And C Virus Antigens |
| Applicant | ALERE SCARBOROUGH, INC D/B/A BINAX, INC. 10 Southgate Rd Scarborough, ME 04074 |
| Contact | Angela Drysdale |
| Correspondent | Angela Drysdale ALERE SCARBOROUGH, INC D/B/A BINAX, INC. 10 Southgate Rd Scarborough, ME 04074 |
| Product Code | PSZ |
| CFR Regulation Number | 866.3328 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-11-07 |
| Decision Date | 2013-12-18 |
| Summary: | summary |