Synergetics, Inc.
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE
SKU K113857UPC HQB
In Stock
—
IIFDA 510(k) Cleared (K113857)
1
Free shipping on orders over $99 · 30-day returns
Synergetics, Inc.
Free shipping on orders over $99 · 30-day returns
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE is an FDA 510(k)-cleared medical device (K113857) manufactured by Synergetics, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 2012. Regulation: 8.
