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Medline ReNewal Reprocessed Nellcor OxiMax SpO2 Sensor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201699
510(k) Type
Special
Applicant
Surgical Instrument and Savings Inc (dba Medline ReNewal)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2020
Days to Decision
30 days
Submission Type
Summary

Medline ReNewal Reprocessed Nellcor OxiMax SpO2 Sensor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201699
510(k) Type
Special
Applicant
Surgical Instrument and Savings Inc (dba Medline ReNewal)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2020
Days to Decision
30 days
Submission Type
Summary