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PRIMA OXYGEN MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010318
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/23/2001
Days to Decision
171 days
Submission Type
Summary

PRIMA OXYGEN MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010318
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/23/2001
Days to Decision
171 days
Submission Type
Summary