Permaseal— 510(k) DEN150029
UnknownMicro Interventional Devices,Inc.
FDA 510(k) clearance DEN150029 for Permaseal, Unknown on 2016-07-27. Applicant: Micro Interventional Devices,Inc.. Device class: 2.
Clearance details
- Applicant
- Micro Interventional Devices,Inc.
- Product code
- Code PNQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.4510
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Newtown, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.