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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name chamber, hyperbaric
510(k) Number K962869
Device Name GSP1 - GAS SELECTION PANEL
Applicant
REIMERS SYSTEMS, INC.
7668 FULLERTON RD., SUITE I-4
SPRINGFIELD,  VA  22153
Applicant Contact STEPHEN D REIMERS
Correspondent
REIMERS SYSTEMS, INC.
7668 FULLERTON RD., SUITE I-4
SPRINGFIELD,  VA  22153
Correspondent Contact STEPHEN D REIMERS
Regulation Number868.5470
Classification Product Code
CBF  
Date Received07/23/1996
Decision Date 10/23/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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