Last synced on 14 November 2025 at 11:06 pm

Lumfuse TP

Page Type
Cleared 510(K)
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)
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