The following data is part of a premarket notification filed by Bio-medical Research, Ltd. with the FDA for Kneehab Xp Conductive Garment, Type 411.
Device ID | K083105 |
510k Number | K083105 |
Device Name: | KNEEHAB XP CONDUCTIVE GARMENT, TYPE 411 |
Classification | Stimulator, Muscle, Powered |
Applicant | BIO-MEDICAL RESEARCH, LTD. PARKMORE BUSINESS PARK WEST Galway, IE |
Contact | Anne-marie Keenan |
Correspondent | Anne-marie Keenan BIO-MEDICAL RESEARCH, LTD. PARKMORE BUSINESS PARK WEST Galway, IE |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-10-20 |
Decision Date | 2009-07-24 |
Summary: | summary |