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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cart, emergency, cardiopulmonary (excluding equipment)
510(k) Number K832697
Device Name RMP INTUBATION EQUIP. STORAGE TRAY
Applicant
RMP CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
RMP CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6175
Classification Product Code
BZN  
Date Received08/10/1983
Decision Date 12/27/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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