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USA Instruments Incorporated

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
LATERAL BIOPSY PLATE - For use with the Liberty 9000, 8-Channel Breast Coil. The Lateral B recall (Z-0505-2007)USA Instruments Incorporated2007-02-15
The recalled product is the medial biopsy plate, part #2414342. The biopsy plate is labele recall (Z-0516-2007)USA Instruments Incorporated2007-02-15
The recalled product is the Lateral biopsy plate, part #2414346. The biopsy plate is label recall (Z-0517-2007)USA Instruments Incorporated2007-02-15
The recalled product is the Disposable biopsy plate, part #U1-150131. The biopsy plate is recall (Z-0518-2007)USA Instruments Incorporated2007-02-15
The recalled product is the Large grid biopsy plate, part #2414797. The biopsy plate is la recall (Z-0519-2007)USA Instruments Incorporated2007-02-15
1.5T HD Head Neck Spine Array, Model 2416329, for GE 1.5T Excite MR System. recall (Z-0163-2007)USA Instruments Incorporated2006-11-09
3.0T HD Head Neck Spine Array, Model 2415545, for GE 3.0T Excite MR System. recall (Z-0164-2007)USA Instruments Incorporated2006-11-09

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Every clearance here is in the API, with alerts when new ones post.