ITEM 8.01 OTHER EVENTS
On June 1, 2009, Palomar Medical Technologies, Inc. (the "Company") received
510(k) Over-The-Counter (OTC) clearance from the United States Food and Drug Administration (FDA) for the first home use wrinkle removal laser device. The Company issued a press release announcing this clearance which is filed as Exhibit 99.1 to this Current Report on Form 8-K. The summary description of the event is qualified in its entirety by reference to the FDA notification letter which is also filed as Exhibit 99.2 to this Current Report on Form 8-K.

ITEM 9.01 FINANCIAL STATEMENTS AND EXHIBITS
(c) Exhibits

Number Title 99.1 Press Release dated June 5, 2009 entitled "PALOMAR RECEIVES FDA OVER-THE-COUNTER CLEARANCE FOR A HOME USE WRINKLE REMOVAL LASER DEVICE Clearance Opens Door to Multi-Billion Dollar Home Skin Care Market" 99.2 FDA notification letter