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ASD SINGLE LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K884620
510(k) Type
Traditional
Applicant
BIOSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
17 days

ASD SINGLE LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K884620
510(k) Type
Traditional
Applicant
BIOSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
17 days