Trimedyne, Inc.
OMNIPULSE HOLMIUM LASER SYSTEM, MODEL 1210; OMNIPULSE MAX HOLMIUM LASER SYSTEM, MODEL 1210-VHP AND 1500-A
SKU K002308UPC GEX
In Stock
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IIFDA 510(k) Cleared (K002308)
1
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Trimedyne, Inc.
Free shipping on orders over $99 · 30-day returns
OMNIPULSE HOLMIUM LASER SYSTEM, MODEL 1210; OMNIPULSE MAX HOLMIUM LASER SYSTEM, MODEL 1210-VHP AND 1500-A is an FDA 510(k)-cleared medical device (K002308) manufactured by Trimedyne, 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 December 19, 2000. Regulation: 8.
