Last synced on 20 December 2024 at 11:05 pm

FLOSHIELD 10MM ENDOSCOPIC CANNULA AND BLUNT OBTURATOR, FLOSHIELD 10MM ENDOSCOPIC CANNULA, FLOSHIELD 10MM BLUNT OBTURATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141272
510(k) Type
Traditional
Applicant
MINIMMALLY INVASIVE DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2014
Days to Decision
112 days
Submission Type
Summary

FLOSHIELD 10MM ENDOSCOPIC CANNULA AND BLUNT OBTURATOR, FLOSHIELD 10MM ENDOSCOPIC CANNULA, FLOSHIELD 10MM BLUNT OBTURATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141272
510(k) Type
Traditional
Applicant
MINIMMALLY INVASIVE DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2014
Days to Decision
112 days
Submission Type
Summary