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MANAN PRO-MAG AUTOMATIC BIOPSY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914874
510(k) Type
Traditional
Applicant
MANAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1992
Days to Decision
112 days
Submission Type
Statement

MANAN PRO-MAG AUTOMATIC BIOPSY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914874
510(k) Type
Traditional
Applicant
MANAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1992
Days to Decision
112 days
Submission Type
Statement