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VALVE, PEEP

Page Type
Cleared 510(K)
510(k) Number
K760230
510(k) Type
Traditional
Applicant
OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1976
Days to Decision
23 days

VALVE, PEEP

Page Type
Cleared 510(K)
510(k) Number
K760230
510(k) Type
Traditional
Applicant
OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1976
Days to Decision
23 days