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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K854022
Device Name LPA-1 PRESSURE MONITOR
Applicant
Life Products, Inc.
2545 Central Ave.
Boulder,  CO  80301
Applicant Contact DOUGLAS BARNES
Correspondent
Life Products, Inc.
2545 Central Ave.
Boulder,  CO  80301
Correspondent Contact DOUGLAS BARNES
Date Received09/30/1985
Decision Date 12/24/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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