Nidek, Inc.
NIDEK MODEL AKC-8000 OPHTHALMIC LASER PHOTOCOAGULA
SKU K900890UPC GEX
In Stock
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IIFDA 510(k) Cleared (K900890)
1
Free shipping on orders over $99 · 30-day returns
Nidek, Inc.
Free shipping on orders over $99 · 30-day returns
NIDEK MODEL AKC-8000 OPHTHALMIC LASER PHOTOCOAGULA is an FDA 510(k)-cleared medical device (K900890) manufactured by Nidek, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 9, 1990. Regulation: 8.
