ClearanceBrief
Company ยท US

Mectra Labs, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2012. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HIFInsufflator, Laparoscopic3
GCJLaparoscope, General & Plastic Surgery2
GEIElectrosurgical, Cutting & Coagulation & Accessories2
HINCoagulator-Cutter, Endoscopic, Bipolar (And Accessories)1
OCTAnti Fog Solution And Accessories, Endoscopy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 29, 2012K113080TUBALGATOR
Mectra Labs, Inc.
HIN
Mar 10, 2004K033880ELECTRO-LUBE
Mectra Labs, Inc.
GEI
Nov 8, 2002K021247PNEUMOPERITONEUM INSUFFLATION NEEDLE
Mectra Labs, Inc.
HIF
Mar 3, 2000K993604ENDOSCOPIC ANTI FOG DEVICE
Mectra Labs, Inc.
OCT
Apr 5, 1996K955352SUCTION CAUTERY PROBE
Mectra Labs, Inc.
GEI
Feb 18, 1994K934547MECTRA TROCAR
Mectra Labs, Inc.
GCJ
Feb 15, 1994K935382GRASPERS
Mectra Labs, Inc.
GCJ
Sep 23, 1993K925691INSUFFLATION TUBING
Mectra Labs, Inc.
HIF
Jul 13, 1992K920959INSUFFLATOR, LAPAROSCOPIC
Mectra Labs, Inc.
HIF

Latest recalls

DateFirm and productCodeLinked 510(k)
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