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MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010413
510(k) Type
Traditional
Applicant
KONICA MINOLTA SENSING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2001
Days to Decision
171 days
Submission Type
Summary

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010413
510(k) Type
Traditional
Applicant
KONICA MINOLTA SENSING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2001
Days to Decision
171 days
Submission Type
Summary