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MAXO2+, MODEL A AND AE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040484
510(k) Type
Traditional
Applicant
MAXTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2004
Days to Decision
105 days
Submission Type
Summary

MAXO2+, MODEL A AND AE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040484
510(k) Type
Traditional
Applicant
MAXTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2004
Days to Decision
105 days
Submission Type
Summary