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MEGA AMNIOCENTESIS KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915863
510(k) Type
Traditional
Applicant
MEGA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
3/30/1992
Days to Decision
90 days
Submission Type
Statement

MEGA AMNIOCENTESIS KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915863
510(k) Type
Traditional
Applicant
MEGA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
3/30/1992
Days to Decision
90 days
Submission Type
Statement