fda
2 records
FDA Device Recall: ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound miniatur
2025-10-15
Class II — Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
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FDA Device Recall: ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with Ima
2024-11-06
Class II — Epoxy used to seal the edge of the transducer into its paddle exceeded specification. This variability could attenuate the ultrasound signal with a potential impact on the quality of images...
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ny_corps
1 records
NY Corp: IMACOR INC.
2009-02-06
FOREIGN BUSINESS CORPORATION | County: Nassau | Jurisdiction: Delaware
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