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REPROCESSED PULSE OXIMETER SENSORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012677
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
591 days
Submission Type
Summary

REPROCESSED PULSE OXIMETER SENSORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012677
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
591 days
Submission Type
Summary