FDA DeviceClass IINotable
FDA Recall: Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
Description
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Hazard
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Remedy
75 units
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