This page includes the latest FDA filings for Peter Kelley. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3003630387 |
FEI Number | 3003630387 |
Name | Peter Kelley |
Owner & Operator | Capsule Technologies |
Contact Address | 300 Brickstone Square #203 Andover MA 01810 US |
US Agent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 300 Brickstone Square Suite 203 Andover, MA 01810 US |
Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
---|---|---|
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus | 2019-05-28 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus | 2019-05-28 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus | 2019-05-28 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus | 2019-05-28 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2018-11-01 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2018-11-01 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2018-11-01 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2018-11-01 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2017-11-20 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2017-11-20 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2017-11-20 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2017-11-20 |
Peter Kelley [Capsule Technologies] | SmartLinx Vitals Plus Patient Monitoring System | 2015-11-17 |