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MEGA PERICARDIOCENTESIS KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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