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3420 DIGIT PULSE OXIMETER, MODEL 3420

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013171
510(k) Type
Traditional
Applicant
BCI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2002
Days to Decision
101 days
Submission Type
Summary

3420 DIGIT PULSE OXIMETER, MODEL 3420

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013171
510(k) Type
Traditional
Applicant
BCI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2002
Days to Decision
101 days
Submission Type
Summary