Wm.I.Kern & Co., Inc.
PBI MULTILASE D COPPER VAPOR LASER
SKU K920004UPC GEX
In Stock
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IIFDA 510(k) Cleared (K920004)
1
Free shipping on orders over $99 · 30-day returns
Wm.I.Kern & Co., Inc.
Free shipping on orders over $99 · 30-day returns
PBI MULTILASE D COPPER VAPOR LASER is an FDA 510(k)-cleared medical device (K920004) manufactured by Wm.I.Kern & Co., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 13, 1992. Regulation: 8.
