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RUSCH BRILLANT SILICONE FOLEY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972184
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1998
Days to Decision
212 days
Submission Type
Summary

RUSCH BRILLANT SILICONE FOLEY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972184
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1998
Days to Decision
212 days
Submission Type
Summary