Last synced on 25 November 2022 at 11:04 pm

MR810 System, 900MR810 Adult Single Limb Circuit, 900MR810E Adult Dual Limb Circuit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143646
510(k) Type
Traditional
Applicant
Fisher & Paykel Healthcare Ltd
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
3/5/2015
Days to Decision
73 days
Submission Type
Summary

MR810 System, 900MR810 Adult Single Limb Circuit, 900MR810E Adult Dual Limb Circuit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143646
510(k) Type
Traditional
Applicant
Fisher & Paykel Healthcare Ltd
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
3/5/2015
Days to Decision
73 days
Submission Type
Summary