
Cooper Lasersonics, Inc.
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MODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROL is an FDA 510(k)-cleared medical device (K844440) manufactured by Cooper Lasersonics, Inc.. This device is classified under the Unknown specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 8, 1985.

Ansell
SKU MSC846624

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SKU VM-1270030

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