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MECTA Corporation

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30205333020533MECTA Corporation1N2020-04-2519799 SW 95TH AVE SUITE B TUALATIN OR US 97062

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00861539000103spECTrum - 100 Joule ECT Device with 4 Parameter Setting Controls and Patient Monitoring(503) 612-6780info@mectacorp.com
00861539000110spECTrum - 100 Joule ECT Device with 1 Parameter Setting Control and Patient Monitoring(503) 612-6780info@mectacorp.com
00861539000127spECTrum - 100 Joule ECT Device with 4 Parameter Setting Controls(503) 612-6780info@mectacorp.com
00861539000134spECTrum - 100 Joule ECT Device with 1 Parameter Setting Control(503) 612-6780info@mectacorp.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
86201020620591K965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.QGH1997-03-06
86201822458315

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QGH11997-03-06

PMN#

GUDID#