510(k) K240162
- Device
- LIFEPAK® 35 AC Power Adapter (41335-000001)
- Applicant
- Stryker Physio-Control
- 510(k) number
- K240162
- Product code
- MPD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2024-04-19
- Date received
- 2024-01-22
- Regulation
- 870.5300
- Classification name
- Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Roshonda Knight
- Address
- 11811 Willows Rd. NE Redmond WA US 98052 98052
FDA Registration Numbers#
- 3015876