Kuraray America, Inc.
MODIFICATION TO PANAVIA F
SKU K002322UPC EMA
In Stock
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IIFDA 510(k) Cleared (K002322)
1
Free shipping on orders over $99 · 30-day returns
Kuraray America, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO PANAVIA F is an FDA 510(k)-cleared medical device (K002322) manufactured by Kuraray America, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2000. Regulation: 8.
