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VENTLAB 6000 SERIES HUMIDIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093617
510(k) Type
Traditional
Applicant
Ventlab Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2011
Days to Decision
430 days
Submission Type
Statement

VENTLAB 6000 SERIES HUMIDIFIER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093617
510(k) Type
Traditional
Applicant
Ventlab Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2011
Days to Decision
430 days
Submission Type
Statement