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PARTNER SEVEN DISP. BUBBLE OXYGENATOR

Page Type
Cleared 510(K)
510(k) Number
K800555
510(k) Type
Traditional
Applicant
CARDIOVASCULAR RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1980
Days to Decision
23 days

PARTNER SEVEN DISP. BUBBLE OXYGENATOR

Page Type
Cleared 510(K)
510(k) Number
K800555
510(k) Type
Traditional
Applicant
CARDIOVASCULAR RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1980
Days to Decision
23 days