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RESUSCITATOR MODELS 10400/10500/10600/10700/10800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862192
510(k) Type
Traditional
Applicant
U.O. EQUIPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1986
Days to Decision
28 days

RESUSCITATOR MODELS 10400/10500/10600/10700/10800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862192
510(k) Type
Traditional
Applicant
U.O. EQUIPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1986
Days to Decision
28 days