E275

Stimulator, Nerve, Transcutaneous, For Pain Relief

MICRO CURRENT TECHNOLOGY, INC.

The following data is part of a premarket notification filed by Micro Current Technology, Inc. with the FDA for E275.

Pre-market Notification Details

Device IDK032653
510k NumberK032653
Device Name:E275
ClassificationStimulator, Nerve, Transcutaneous, For Pain Relief
Applicant MICRO CURRENT TECHNOLOGY, INC. 4822 CALIFORNIA AVE., S.W., SUITE 201 Seattle,  WA  98116
ContactDavid Suzuki
CorrespondentMarc M Mouser
UNDERWRITERS LABORATORIES, INC. 2600 NW LAKE RD. Camas,  WA  98607 -9526
Product CodeGZJ  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedYes
Combination ProductNo
Date Received2003-08-28
Decision Date2003-09-12

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00817076010853 K032653 000
00817076010822 K032653 000

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