The following data is part of a premarket notification filed by Masimo Corporation with the FDA for Masimo Radical Y Pulse Co-oximeter.
Device ID | K110028 |
510k Number | K110028 |
Device Name: | MASIMO RADICAL Y PULSE CO-OXIMETER |
Classification | Oximeter |
Applicant | MASIMO CORPORATION 40 PARKER Irvine, CA 92618 |
Contact | Shelly Harris |
Correspondent | Shelly Harris MASIMO CORPORATION 40 PARKER Irvine, CA 92618 |
Product Code | DQA |
Subsequent Product Code | BZQ |
Subsequent Product Code | DPZ |
Subsequent Product Code | JKS |
CFR Regulation Number | 870.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-01-05 |
Decision Date | 2011-03-17 |
Summary: | summary |