ClearanceBrief
Company ยท US

Mecta Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 2021. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QGHElectroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder4
JXLBlock, Bite1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 4, 2021K201309ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size Medium
Mecta Corporation
JXL
Apr 26, 2020K192834MECTA Sigma
Mecta Corporation
QGH
Mar 6, 1997K965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.
Mecta Corp.
QGH
Sep 18, 1996K960754SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M
Mecta Corp.
QGH
Aug 9, 1985K852069MECTA ECT DEVICE MODELS SR & JR
Mecta Corp.
QGH

Latest recalls

DateFirm and productCodeLinked 510(k)
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