Peter Kelley

FDA Filings

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.

FDA Registration(s)
Registration Number3003630387
FEI Number3003630387
NamePeter Kelley
Owner & OperatorCapsule Technologies
Contact Address300 Brickstone Square #203
Andover MA 01810 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address300 Brickstone Square Suite 203
Andover, MA 01810 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus2019-05-28
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus2019-05-28
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus2019-05-28
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus2019-05-28
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2018-11-01
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2018-11-01
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2018-11-01
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2018-11-01
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2017-11-20
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2017-11-20
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2017-11-20
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2017-11-20
Peter Kelley [Capsule Technologies]
SmartLinx Vitals Plus Patient Monitoring System2015-11-17

Similar & Related FDA Registered Companies

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.