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INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960883
510(k) Type
Traditional
Applicant
TAUT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1996
Days to Decision
15 days
Submission Type
Statement