FDA 510(k) Applications Submitted by CHARLES E ALLGOOD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K021247	04/19/2002	PNEUMOPERITONEUM INSUFFLATION NEEDLE	MECTRA LABS, INC.
K113080	10/18/2011	TUBALGATOR	MECTRA LABS, INC.
K993604	10/25/1999	ENDOSCOPIC ANTI FOG DEVICE	MECTRA LABS, INC.
K955352	11/21/1995	SUCTION CAUTERY PROBE	MECTRA LABS, INC.
K033880	12/15/2003	ELECTRO-LUBE	MECTRA LABS, INC.