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PROSTATE BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K982401
510(k) Type
Traditional
Applicant
REMINGTON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1998
Days to Decision
60 days
Submission Type
Statement

PROSTATE BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K982401
510(k) Type
Traditional
Applicant
REMINGTON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1998
Days to Decision
60 days
Submission Type
Statement