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BIP BIOPSY NEEDLE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K934370
510(k) Type
Traditional
Applicant
BIP USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
181 days
Submission Type
Statement

BIP BIOPSY NEEDLE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K934370
510(k) Type
Traditional
Applicant
BIP USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
181 days
Submission Type
Statement