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OHIO MODEL 922 SPIROMETER

Page Type
Cleared 510(K)
510(k) Number
K832185
510(k) Type
Traditional
Applicant
AIRCO/OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
37 days

OHIO MODEL 922 SPIROMETER

Page Type
Cleared 510(K)
510(k) Number
K832185
510(k) Type
Traditional
Applicant
AIRCO/OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1983
Days to Decision
37 days