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MR810RESPIRATORY HUMIDIFIER, 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
K131957
510(k) Type
Traditional
Applicant
FISHER & PAYKEL HEALTHCARE, LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
160 days
Submission Type
Summary

MR810RESPIRATORY HUMIDIFIER, 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
K131957
510(k) Type
Traditional
Applicant
FISHER & PAYKEL HEALTHCARE, LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
160 days
Submission Type
Summary