Last synced on 25 January 2026 at 3:41 am

Pluski Safe 1 Safety IV Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210037
510(k) Type
Traditional
Applicant
Mediplus (India) Limited
Country
India
FDA Decision
Substantially Equivalent
Decision Date
3/25/2022
Days to Decision
443 days
Submission Type
Summary

Pluski Safe 1 Safety IV Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210037
510(k) Type
Traditional
Applicant
Mediplus (India) Limited
Country
India
FDA Decision
Substantially Equivalent
Decision Date
3/25/2022
Days to Decision
443 days
Submission Type
Summary