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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Image Processing, Radiological
510(k) Number K890397
Device Name REDI-VU MODEL RV-386
Applicant
J.D. Technical Services
2455-G Autumnvale Dr.
San Jose,  CA  95131
Applicant Contact JERRY PEPMUELLER
Correspondent
J.D. Technical Services
2455-G Autumnvale Dr.
San Jose,  CA  95131
Correspondent Contact JERRY PEPMUELLER
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received01/24/1989
Decision Date 04/14/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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