Argon Medical Devices, Inc.
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
SKU K191758UPC MMX
In Stock
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IIFDA 510(k) Cleared (K191758)
1
Free shipping on orders over $99 · 30-day returns
Argon Medical Devices, Inc.
Free shipping on orders over $99 · 30-day returns
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is an FDA 510(k)-cleared medical device (K191758) manufactured by Argon Medical Devices, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 2019. Regulation: 8.
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