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MEGA PERICARDIOCENTESIS KIT

Page Type
Cleared 510(K)
510(k) Number
K912564
510(k) Type
Traditional
Applicant
MEGA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1991
Days to Decision
86 days
Submission Type
Statement

MEGA PERICARDIOCENTESIS KIT

Page Type
Cleared 510(K)
510(k) Number
K912564
510(k) Type
Traditional
Applicant
MEGA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1991
Days to Decision
86 days
Submission Type
Statement