COM-PATCH

Electrode, Cutaneous

APEX MEDICAL CORP.

The following data is part of a premarket notification filed by Apex Medical Corp. with the FDA for Com-patch.

Pre-market Notification Details

Device IDK012140
510k NumberK012140
Device Name:COM-PATCH
ClassificationElectrode, Cutaneous
Applicant APEX MEDICAL CORP. 10TH FLOOR, NO.31, LANE 169 KANG NING STREET Hsi-chih City, Taipei Hsien,  TW
ContactAlan Chang
CorrespondentAlan Chang
APEX MEDICAL CORP. 10TH FLOOR, NO.31, LANE 169 KANG NING STREET Hsi-chih City, Taipei Hsien,  TW
Product CodeGXY  
CFR Regulation Number882.1320 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-07-10
Decision Date2001-10-05

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