Last synced on 20 December 2024 at 11:05 pm

DIRECTVIEW, LIGHTGUIDE, MODEL(S) 10RLL-320 LAPAROSCOPE, 10DLG-320 DISPOSABLE LIGHT GUIDE FOR ABOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072613
510(k) Type
Traditional
Applicant
MICRO INVASIVE TECHNOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2008
Days to Decision
217 days
Submission Type
Summary

DIRECTVIEW, LIGHTGUIDE, MODEL(S) 10RLL-320 LAPAROSCOPE, 10DLG-320 DISPOSABLE LIGHT GUIDE FOR ABOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072613
510(k) Type
Traditional
Applicant
MICRO INVASIVE TECHNOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2008
Days to Decision
217 days
Submission Type
Summary