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RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892885
510(k) Type
Traditional
Applicant
FISHER & PAYKEL ELECTRONICS LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
10/6/1989
Days to Decision
170 days

RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892885
510(k) Type
Traditional
Applicant
FISHER & PAYKEL ELECTRONICS LTD.
Country
New Zealand
FDA Decision
Substantially Equivalent
Decision Date
10/6/1989
Days to Decision
170 days