Medical Device Recalls
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1 result found
510(K) Number: K854244 |
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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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Keeler All Pupil II Indirect Ophthalmoscope, Keeler Instruments, Inc., Broomall, PA 19008 | 2 | 05/22/2008 | Keeler Instruments Inc |
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