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INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K830609
510(k) Type
Traditional
Applicant
INTERVENTIONAL MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
27 days

INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K830609
510(k) Type
Traditional
Applicant
INTERVENTIONAL MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
27 days