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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrode, Cutaneous
510(k) Number K872976
Device Name TENS PALS PLUS
Applicant
Axelgaard Mfg. Co., Ltd.
2302 Martin St.
Suite 320
Irvine,  CA  92715
Applicant Contact WALTER A HACKLER
Correspondent
Axelgaard Mfg. Co., Ltd.
2302 Martin St.
Suite 320
Irvine,  CA  92715
Correspondent Contact WALTER A HACKLER
Regulation Number882.1320
Classification Product Code
GXY  
Date Received07/30/1987
Decision Date 09/22/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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