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Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181738
510(k) Type
Traditional
Applicant
Surgical Instrument Service and Savings Inc (dba Medline
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
263 days
Submission Type
Summary

Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181738
510(k) Type
Traditional
Applicant
Surgical Instrument Service and Savings Inc (dba Medline
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
263 days
Submission Type
Summary