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Intermittent nelaton catheter for single use

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222677
510(k) Type
Traditional
Applicant
Hangzhou Jimushi Meditech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/5/2023
Days to Decision
211 days
Submission Type
Summary

Intermittent nelaton catheter for single use

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222677
510(k) Type
Traditional
Applicant
Hangzhou Jimushi Meditech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/5/2023
Days to Decision
211 days
Submission Type
Summary