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CARDIOVUE ACCESSORY CART

Page Type
Cleared 510(K)
510(k) Number
K820033
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
16 days

CARDIOVUE ACCESSORY CART

Page Type
Cleared 510(K)
510(k) Number
K820033
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
16 days