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MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862923
510(k) Type
Traditional
Applicant
FISHER & PAYKEL ALLIED PRODUCTS LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
9/23/1986
Days to Decision
53 days

MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862923
510(k) Type
Traditional
Applicant
FISHER & PAYKEL ALLIED PRODUCTS LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
9/23/1986
Days to Decision
53 days