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SYMBIOSIS BONE MARROW BIOPSY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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