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CPAP SYSTEM, MODEL 102001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001318
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2000
Days to Decision
85 days
Submission Type
Summary

CPAP SYSTEM, MODEL 102001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001318
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2000
Days to Decision
85 days
Submission Type
Summary