The following data is part of a premarket notification filed by Reflectance Medical Inc with the FDA for Multi-parameter Mobile Careguide 3100 Oximeter.
Device ID | K130079 |
510k Number | K130079 |
Device Name: | MULTI-PARAMETER MOBILE CAREGUIDE 3100 OXIMETER |
Classification | Oximeter, Tissue Saturation |
Applicant | REFLECTANCE MEDICAL INC 116 FLAUNDERS ROAD, SUITE 1000 Westborough, MA 01581 |
Contact | Nandini Murthy |
Correspondent | Nandini Murthy REFLECTANCE MEDICAL INC 116 FLAUNDERS ROAD, SUITE 1000 Westborough, MA 01581 |
Product Code | MUD |
CFR Regulation Number | 870.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-01-14 |
Decision Date | 2013-07-19 |
Summary: | summary |