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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name oximeter
510(k) Number K914538
Device Name UPH-2000 UNIVERSAL OXIMETRY PROBE HOLDER
Applicant
INNOVATIVE MEDICAL PRODUCTS, INC.
825 ROSELAND PKWY.
HRAHAN,  LA  70123
Applicant Contact CHARLES D MAYEUX
Correspondent
INNOVATIVE MEDICAL PRODUCTS, INC.
825 ROSELAND PKWY.
HRAHAN,  LA  70123
Correspondent Contact CHARLES D MAYEUX
Regulation Number870.2700
Classification Product Code
DQA  
Date Received10/11/1991
Decision Date 07/14/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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