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Lumfuse TP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173189
510(k) Type
Traditional
Applicant
Precifit Medical Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2018
Days to Decision
249 days
Submission Type
Summary

Lumfuse TP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173189
510(k) Type
Traditional
Applicant
Precifit Medical Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2018
Days to Decision
249 days
Submission Type
Summary