510(k) K002258

Device
ULTRAGUIDE CT-GUIDE 1010
Applicant
ULTRAGUIDE LTD.
510(k) number
K002258
Product code
JAK  
Decision
Substantially Equivalent (SESE)
Decision date
2000-08-08
Date received
2000-07-25
Regulation
892.1750
Classification name
System, X-ray, Tomography, Computed
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
GEORGE MYERS
Address
377 Rte. 17 S. Hasbrouck Heights NJ US 07601 07601

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code JAK  

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K253596Aquilion ONE (TSX-308A/TSX-306A) V2.0Canon Medical Systems Corporation2026-05-20
K253649Spectral CT Verida FamilyPhilips Medical Systems Technologies , Ltd.2026-03-27
K253686True Definition DLGe Healthcare Japan Corporation2026-03-23
K252992CT Rembra RT; CT Areta RT; CT RembraPhilips Healthcare (Suzhou) Co., Ltd.2026-03-23
K253574SOMATOM X.cite; SOMATOM X.ceedSiemens Medical Solutions USA, Inc.2026-03-20
K253520Photonova Spectra, Photonova Spectra SelectGe Medical Systems, LLC2026-03-20
K260078Aquilion ServeSP (TSX-307B) V2.0Canon Medical Systems Corporation2026-03-13
K252249Extremity CT Imaging SystemMars Bioimaging , Ltd.2026-03-13
K260167Bunkerhill Contrast AVCBunkerHill Health2026-03-06
K260166Bunkerhill Contrast CACBunkerHill Health2026-03-06
K260169AV Cardiac CTPhilips Medical Systems Nederland B.V.2026-03-05
K253173uCT 780 with uWS-CT-Dual Energy AnalysisShanghai United Imaging Healthcare Co., Ltd.2026-01-20
K252217CT VScore+Canon Medical Informatics, Inc.2025-11-28
K251805syngo.CT Dual EnergySiemens Medical Solutions USA, Inc.2025-10-15
K250662Bunkerhill MACBunkerHill Health2025-10-03

Legacy Summary

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FDA Review

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