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MR810RESPIRATORY HUMIDIFIER, 900MR810 ADULT SINGLE LIMB CIRCUIT, 900MR810E ADULT DUAL LIMB CIRCUIT

Page Type
Cleared 510(K)
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)
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