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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 K951125
Device Name LIFEFORCE CLINICAL HYPERBARIC FACILITY
Applicant
Reimers Systems, Inc.
7668 Fullerton Rd., Suite I-4
Springfield,  VA  22153
Applicant Contact BENJAMIN D TICE
Correspondent
Reimers Systems, Inc.
7668 Fullerton Rd., Suite I-4
Springfield,  VA  22153
Correspondent Contact BENJAMIN D TICE
Regulation Number868.5470
Classification Product Code
CBF  
Date Received03/13/1995
Decision Date 06/02/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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