Nidacon International AB
MODIFICATION OF PURESPERM
SKU K984172UPC MQL
In Stock
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IIFDA 510(k) Cleared (K984172)
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Free shipping on orders over $99 · 30-day returns
Nidacon International AB
Free shipping on orders over $99 · 30-day returns
MODIFICATION OF PURESPERM is an FDA 510(k)-cleared medical device (K984172) manufactured by Nidacon International AB. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 1999. Regulation: 8.
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