Last synced on 24 May 2024 at 11:04 pm

PMT Platinum Depthalon Depth Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151790
510(k) Type
Traditional
Applicant
PMT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2016
Days to Decision
379 days
Submission Type
Statement

PMT Platinum Depthalon Depth Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151790
510(k) Type
Traditional
Applicant
PMT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2016
Days to Decision
379 days
Submission Type
Statement