Nidek, Inc.
NIDEK KM-1000 SURGICAL KERATOMETER
SKU K862137UPC HLQ
In Stock
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IFDA 510(k) Cleared (K862137)
1
Free shipping on orders over $99 · 30-day returns
Nidek, Inc.
Free shipping on orders over $99 · 30-day returns
NIDEK KM-1000 SURGICAL KERATOMETER is an FDA 510(k)-cleared medical device (K862137) manufactured by Nidek, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 22, 1986. Regulation: 8.
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