510(k) K011418

Device
ULTRAGUIDE MR-GUIDE 3000
Applicant
ULTRAGUIDE LTD.
510(k) number
K011418
Product code
LNH  
Decision
Substantially Equivalent (SESE)
Decision date
2001-05-24
Date received
2001-05-09
Regulation
892.1000
Classification name
System, Nuclear Magnetic Resonance Imaging
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

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Legacy Summary

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FDA Review

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