Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K200435 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-00... | 2 | 01/14/2026 | C-RAD POSITIONING AB |
| Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-00... | 2 | 05/28/2025 | C-RAD POSITIONING AB |
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