
Inframed, Inc.
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CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE is an FDA 510(k)-cleared medical device (K864610) manufactured by Inframed, Inc.. This device is classified under the Unknown specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 17, 1987.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031