The following data is part of a premarket notification filed by Well-life Healthcare Limited with the FDA for If True Sine Interferential Stimulator, Wl-2206d.
Device ID | K092763 |
510k Number | K092763 |
Device Name: | IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D |
Classification | Interferential Current Therapy |
Applicant | WELL-LIFE HEALTHCARE LIMITED 1FL, NO.16, LANE 454 JUNGJENG RD. Yunghe City, Taipei County, TW |
Contact | Jenny Hsieh |
Correspondent | Jenny Hsieh WELL-LIFE HEALTHCARE LIMITED 1FL, NO.16, LANE 454 JUNGJENG RD. Yunghe City, Taipei County, TW |
Product Code | LIH |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-09-09 |
Decision Date | 2009-10-08 |
Summary: | summary |