Last synced on 2 December 2022 at 11:04 pm

Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183461
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/8/2019
Days to Decision
145 days
Submission Type
Summary

Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183461
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/8/2019
Days to Decision
145 days
Submission Type
Summary