Haag-Streit USA Inc
4 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to det recall (Z-2411-2012) | Haag-Streit USA Inc | 2012-09-20 |
| Octopus 900 Perimeter, EyeSuite Perimetry version i4.000 (Flash v. 2.1.4 & 2.1.5), Model N recall (Z-0638-2012) | Haag-Streit USA Inc | 2012-01-11 |
| Lenstar LS 900 EyeSuite Biometry version i2.000, Four (4) Protective Cardboard Containers recall (Z-2964-2011) | Haag-Streit USA Inc | 2011-08-09 |
| Lenstar LS 900, Biomicroscope, Slit-Lamp, AC-powered. HAAG-STREIT AG, Switzerland. Used fo recall (Z-1897-2010) | Haag-Streit USA Inc | 2010-06-24 |
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Every clearance here is in the API, with alerts when new ones post.