Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K071619 |
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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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Sterile Drape, SK6000 PAQ drape pouch (for use with the SPY Fluorescent System (SPY 2000/2001)) T... | 2 | 09/08/2016 | NOVADAQ TECHNOLOGIES INC. |
LUNA Chest, Model No. LU4006 | 3 | 12/01/2014 | Novadaq Technologies, Inc. |
Non-sterile drape | 3 | 12/01/2014 | Novadaq Technologies, Inc. |
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