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FDA 510(k) Applications Submitted by MECTRA LABS, INC.
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.
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