
Keeler Instruments, Inc.
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PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000 is an FDA 510(k)-cleared medical device (K093298) manufactured by Keeler Instruments, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 9, 2010. Regulation: 8.