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SYMBIOSIS BONE MARROW BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K925416
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1993
Days to Decision
119 days
Submission Type
Statement

SYMBIOSIS BONE MARROW BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K925416
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1993
Days to Decision
119 days
Submission Type
Statement