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DAUM NEUROCUT NEUROBIOPSYNEEDLE

Page Type
Cleared 510(K)
510(k) Number
K990278
510(k) Type
Traditional
Applicant
DAUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1999
Days to Decision
61 days
Submission Type
Statement

DAUM NEUROCUT NEUROBIOPSYNEEDLE

Page Type
Cleared 510(K)
510(k) Number
K990278
510(k) Type
Traditional
Applicant
DAUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1999
Days to Decision
61 days
Submission Type
Statement