FDA 510(k) Applications Submitted by JAY CAPLAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K981351	04/14/1998	CANDELA GENTLELASE GL DERMATOLOGICAL LASER	CANDELA CORP.
K972767	07/24/1997	CANDELA GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER	CANDELA CORP.
K955662	12/12/1995	CANDELA Q-SWITCHED ALEXANDRITE LASERS	CANDELA LASER CORP.
K994260	12/17/1999	CANDELA GENTLELASE GL DERMATOLOGICAL LASER	CANDELA CORP.
K984601	12/28/1998	CANDELA GENTLELASE II DERMATOLOGICAL LASER	CANDELA CORP.