The following data is part of a premarket notification filed by Masimo Corp. with the FDA for Modification To Masimo Set Radical Pulse Oximeter With Satshare And Lnop Series Of Senors Oximeter.
Device ID | K002939 |
510k Number | K002939 |
Device Name: | MODIFICATION TO MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE AND LNOP SERIES OF SENORS OXIMETER |
Classification | Oximeter |
Applicant | MASIMO CORP. 2852 KELVIN AVE. Irvine, CA 92614 -5826 |
Contact | James J Cronin |
Correspondent | James J Cronin MASIMO CORP. 2852 KELVIN AVE. Irvine, CA 92614 -5826 |
Product Code | DQA |
CFR Regulation Number | 870.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-21 |
Decision Date | 2000-10-06 |