FDA DeviceClass IINotable
FDA Recall: Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440
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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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
27 units
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