Stereo Navigator Accessory, STN-1000

FDA 510(k) K082354 · Naviscan Pet Systems

Substantially Equivalent

510(k) numberK082354

Submission

Device name
Stereo Navigator Accessory, STN-1000
Applicant
Naviscan Pet Systems
San Diego, CA, US
Received
August 15, 2008
Decision date
November 18, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KPS – System, Tomography, Computed, Emission
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1200
Specialty
Radiology

Other 510(k)s with product code KPS

510(k)DeviceApplicantDecision
K261305Micsi-PetKPS · Traditional Microstructure Imaging, Inc.09/11/2026SE
K261427uMI Panvivo (uMI Panvivo M)KPS · Traditional Shanghai United Imaging Healthcare Co., Ltd.07/28/2026SE
K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7…KPS · Special Siemens Medical Solutions USA, Inc.05/21/2026SE
K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S)…KPS · Traditional Shanghai United Imaging Healthcare Co., Ltd.04/03/2026SE
K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX)…KPS · Traditional Shanghai United Imaging Healthcare Co., Ltd.02/13/2026SE
K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400…KPS · Special Spectrum Dynamics Medical, Ltd.01/13/2026SE
K253844AnyScan 3.0 NM Scanner FamilyKPS · Traditional Mediso Medical Imaging Systems, Ltd.12/30/2025SE
K251370Cartesion Prime (PCD-1000A/3) V10.21KPS · Traditional Canon Medical Systems Corporation12/01/2025SE
K251401PennPET Explorer Positron Emission TomographKPS · Traditional Trustees of the University of Pennsylvania11/25/2025SE
K252477Hybrid Viewer (00859873006240)KPS · Special Hermes Medical Solutions AB09/09/2025SE

Questions and answers

When was Stereo Navigator Accessory, STN-1000 cleared by the FDA?

Stereo Navigator Accessory, STN-1000 (K082354) received a 510(k) decision of Substantially Equivalent on November 18, 2008, 95 days after the submission was received.

What is the product code of K082354?

The FDA product code is KPS – System, Tomography, Computed, Emission, a Class II (moderate risk) device regulated under 21 CFR 892.1200.