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Q220F CARDITOMY RESERVOIR/MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K790635
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1979
Days to Decision
16 days

Q220F CARDITOMY RESERVOIR/MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K790635
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1979
Days to Decision
16 days