Last synced on 23 September 2022 at 11:05 pm

ENDOPLUS hand-held laparoscopic instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151567
510(k) Type
Traditional
Applicant
ENDOPLUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2015
Days to Decision
196 days
Submission Type
Summary

ENDOPLUS hand-held laparoscopic instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151567
510(k) Type
Traditional
Applicant
ENDOPLUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2015
Days to Decision
196 days
Submission Type
Summary