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ATRAUMATIC SPECIAL SPROTTE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911221
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1992
Days to Decision
493 days

ATRAUMATIC SPECIAL SPROTTE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911221
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1992
Days to Decision
493 days