Olympus America, Inc.
HI-Q HAND INSTRUMENTS, OB/GYN USE
SKU K944200UPC HET
In Stock
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IIFDA 510(k) Cleared (K944200)
1
Free shipping on orders over $99 · 30-day returns
Olympus America, Inc.
Free shipping on orders over $99 · 30-day returns
HI-Q HAND INSTRUMENTS, OB/GYN USE is an FDA 510(k)-cleared medical device (K944200) manufactured by Olympus America, Inc.. 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 September 14, 1995. Regulation: 8.
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