Medical Device Manufacturer · US , Portland , OR

Mecta Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1985
3
Total
3
Cleared
0
Denied

Mecta Corp. has 3 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 3 cleared submissions from 1985 to 1997. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Mecta Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mecta Corp.

3 devices
1-3 of 3
Cleared Mar 06, 1997
SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.
K965070 · QGH
Neurology · 85d
Cleared Sep 18, 1996
SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M
K960754 · QGH
Neurology · 208d
Cleared Aug 09, 1985
MECTA ECT DEVICE MODELS SR & JR
K852069 · QGH
Neurology · 91d
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All3 Neurology 3