The following data is part of a premarket notification filed by Masimo Corp. with the FDA for Masimo Set Ms-1p Pulse Oximeter And The Lnop Series Of Sensors And Cables.
Device ID | K973887 |
510k Number | K973887 |
Device Name: | MASIMO SET MS-1P PULSE OXIMETER AND THE LNOP SERIES OF SENSORS AND CABLES |
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 | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-10-14 |
Decision Date | 1998-01-08 |
Summary: | summary |