FDA 510(k) Applications Submitted by PETER CHUN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090910	04/01/2009	HANSO ACUPUNCTURE NEEDLE	HANSOL MEDICAL CO.
K092831	09/15/2009	DISPOSABLE HYPODERMIC NEEDLE	FEEL TECH
K100045	01/08/2010	OCTO	DALIM SURGNET CORPORATION
K120460	02/15/2012	SMARTLUX	MEDMIX CO., LTD
K120471	02/16/2012	MACH BRACKETS BRIGHT BRACKETS	WORLD BIO TECH CO., LTD
K120545	02/23/2012	HX-461	SEERS TECHNOLOGY CO, LTD
K140458	02/24/2014	DIOTECH LASER FIBER	DIOTECH CO
K110881	03/30/2011	ULTRASONIC SURGICAL UNIT	DONG IL TECHNOLOGY LTD.
K111392	05/18/2011	WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)	WOOJEON COMPANY
K141715	06/25/2014	GLOVE PORT	NELIS
K112153	07/07/2011	IROOT 100 MINI	S-DENTI CO., LTD.
K101912	07/09/2010	THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301	HUBDIC CO., LTD
K112332	08/12/2011	FINE JECT INSULIN PEN NEEDLE	TWOBIENS CO., LTD.