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BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K101832
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
57 days
Submission Type
Summary

BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K101832
510(k) Type
Traditional
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
57 days
Submission Type
Summary