Kelsey, Inc.
KELSEY INTERSITITAL LASER THERAPY SYSTEM
SKU K070353UPC GEX
In Stock
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IIFDA 510(k) Cleared (K070353)
1
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Kelsey, Inc.
Free shipping on orders over $99 · 30-day returns
KELSEY INTERSITITAL LASER THERAPY SYSTEM is an FDA 510(k)-cleared medical device (K070353) manufactured by Kelsey, 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 1, 2007. Regulation: 8.
