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ADULT RESUSCITATOR WITH MASK AND FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884526
510(k) Type
Traditional
Applicant
INTERTECH/OHIO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1988
Days to Decision
20 days

ADULT RESUSCITATOR WITH MASK AND FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884526
510(k) Type
Traditional
Applicant
INTERTECH/OHIO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1988
Days to Decision
20 days