MEDIPLUS SINGLE USE GI MANOMETRY CATHETER— 510(k) K013704
Substantially EquivalentMediplus , Ltd.
FDA 510(k) clearance K013704 for MEDIPLUS SINGLE USE GI MANOMETRY CATHETER, Substantially Equivalent on 2002-08-05. Applicant: Mediplus , Ltd..
Clearance details
- Applicant
- Mediplus , Ltd.
- Product code
- Code KLA
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Petersburg, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.