Last synced on 16 May 2025 at 11:05 pm

MEDIPLUS SINGLE USE GI MANOMETRY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013704
510(k) Type
Traditional
Applicant
MEDIPLUS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2002
Days to Decision
270 days
Submission Type
Summary

MEDIPLUS SINGLE USE GI MANOMETRY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013704
510(k) Type
Traditional
Applicant
MEDIPLUS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2002
Days to Decision
270 days
Submission Type
Summary