Protocol Systems, Inc.
MICROPAQ, MODELS 402 AND 404
SKU K002725UPC DRT
In Stock
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IIFDA 510(k) Cleared (K002725)
1
Free shipping on orders over $99 · 30-day returns
Protocol Systems, Inc.
Free shipping on orders over $99 · 30-day returns
MICROPAQ, MODELS 402 AND 404 is an FDA 510(k)-cleared medical device (K002725) manufactured by Protocol 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 November 20, 2000. Regulation: 8.
