Last synced on 2 December 2022 at 11:04 pm

ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961392
510(k) Type
Traditional
Applicant
SIL-MED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1997
Days to Decision
463 days
Submission Type
Summary

ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961392
510(k) Type
Traditional
Applicant
SIL-MED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1997
Days to Decision
463 days
Submission Type
Summary