Last synced on 19 July 2024 at 11:05 pm

FLEXICARE FL-9000U RESPIRATORY HUMIDIFIER BASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161314
510(k) Type
Traditional
Applicant
FLEXICARE MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/6/2016
Days to Decision
56 days
Submission Type
Summary

FLEXICARE FL-9000U RESPIRATORY HUMIDIFIER BASE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161314
510(k) Type
Traditional
Applicant
FLEXICARE MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/6/2016
Days to Decision
56 days
Submission Type
Summary