Last synced on 14 June 2024 at 11:05 pm

WECK VISTA OPTICAL BLADELESS LAPAROSCOPIC ACCESS PORT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121380
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2012
Days to Decision
17 days
Submission Type
Summary