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PATIENT VENTILATOR ISOLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880923
510(k) Type
Traditional
Applicant
DRYDEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1988
Days to Decision
186 days

PATIENT VENTILATOR ISOLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880923
510(k) Type
Traditional
Applicant
DRYDEN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1988
Days to Decision
186 days