Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K152531 |
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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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InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile sheath cleans and clears th... | 2 | 05/23/2024 | Olympus Corporation of the Americas |
InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic... | 2 | 03/22/2024 | Olympus Corporation of the Americas |
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