Non-Invasive Monitoring Systems, Inc.
RESPIEVENTS, VERSION 4.2
SKU K001369UPC DQK
In Stock
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IIFDA 510(k) Cleared (K001369)
1
Free shipping on orders over $99 · 30-day returns
Non-Invasive Monitoring Systems, Inc.
Free shipping on orders over $99 · 30-day returns
RESPIEVENTS, VERSION 4.2 is an FDA 510(k)-cleared medical device (K001369) manufactured by Non-Invasive Monitoring Systems, 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 July 25, 2000. Regulation: 8.
