
Surgilase, Inc.
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ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY is an FDA 510(k)-cleared medical device (K875042) manufactured by Surgilase, Inc.. This device is classified under the Unknown specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 23, 1988.

Ansell
SKU MSC846624

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SKU K014192

McKesson
SKU VM-1270030

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SKU VM-1270031