Last synced on 10 January 2025 at 11:05 pm

MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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