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ULTRA-CORE BIOPSY NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921418
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1992
Days to Decision
87 days
Submission Type
Statement

ULTRA-CORE BIOPSY NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921418
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1992
Days to Decision
87 days
Submission Type
Statement