
L.A.S.E.R., Inc.
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DOUBLE PUNCTURE INSTRUMENTS is an FDA 510(k)-cleared medical device (K852901) manufactured by L.A.S.E.R., 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 October 15, 1985. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
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Hollister
SKU VM-1270031