Binax, Inc. dba IMPD
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Inverness Medical BioStar Strep A OIA MAX, 100 test kit size, Product Code: 90003, in vitr recall (Z-1506-2009) | Binax, Inc. dba IMPD | 2009-06-24 |
| BinaxNOW Influenza A&B 10 Test KIT Part Number: 416-110 contains NP Swabs with '8995' labe recall (Z-0822-2007) | Binax, Inc. dba IMPD | 2007-05-23 |
| BinaxNOW Influenza A&B 22 Test Kit Part Number: 416-022, contains NP Swabs with '8995' lab recall (Z-0823-2007) | Binax, Inc. dba IMPD | 2007-05-23 |
| BinaxNOW RSV 10 Test Kit Part Number : 430-100, contains NP Swabs with '8995' labeled on t recall (Z-0824-2007) | Binax, Inc. dba IMPD | 2007-05-23 |
| BinaxNOW Nasopharyngeal (NP) Accessory Pak, Part Number 400-065, contain NP Swabs with '89 recall (Z-0825-2007) | Binax, Inc. dba IMPD | 2007-05-23 |
| BinaxNOW A&B Kit 10 Test Kit (Japan) Part No. 416-110J contains NP Swabs with '8995' label recall (Z-0826-2007) | Binax, Inc. dba IMPD | 2007-05-23 |
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Every clearance here is in the API, with alerts when new ones post.