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ATRAUMATIC STANDARD SPROTTE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911260
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1991
Days to Decision
213 days

ATRAUMATIC STANDARD SPROTTE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911260
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1991
Days to Decision
213 days