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RESUSCITATOR VALVE ASSEMBLY W/FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882204
510(k) Type
Traditional
Applicant
INTERTECH/OHIO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
44 days

RESUSCITATOR VALVE ASSEMBLY W/FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882204
510(k) Type
Traditional
Applicant
INTERTECH/OHIO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
44 days