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TETRAD MODEL BS18, ENDOSURGICAL NEEDLE GUIDE ATTACHMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945319
510(k) Type
Traditional
Applicant
TETRA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1995
Days to Decision
184 days
Submission Type
Statement

TETRAD MODEL BS18, ENDOSURGICAL NEEDLE GUIDE ATTACHMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945319
510(k) Type
Traditional
Applicant
TETRA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1995
Days to Decision
184 days
Submission Type
Statement