The following data is part of a premarket notification filed by Apex Medical Corp. with the FDA for Com-patch.
Device ID | K012140 |
510k Number | K012140 |
Device Name: | COM-PATCH |
Classification | Electrode, Cutaneous |
Applicant | APEX MEDICAL CORP. 10TH FLOOR, NO.31, LANE 169 KANG NING STREET Hsi-chih City, Taipei Hsien, TW |
Contact | Alan Chang |
Correspondent | Alan Chang APEX MEDICAL CORP. 10TH FLOOR, NO.31, LANE 169 KANG NING STREET Hsi-chih City, Taipei Hsien, TW |
Product Code | GXY |
CFR Regulation Number | 882.1320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-07-10 |
Decision Date | 2001-10-05 |