Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K082891 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Lenstar LS 900, Biomicroscope, Slit-Lamp, AC-powered. HAAG-STREIT AG, Switzerland. Used for obtai... | 2 | 06/24/2010 | Haag-Streit USA Inc |
Lenstar LS 900 EyeSuite Biometry version i2.000, Four (4) Protective Cardboard Containers Per Each S... | 2 | 08/09/2011 | Haag-Streit USA Inc |
Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope. | 2 | 05/11/2021 | Haag-Streit USA Inc |
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