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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Battery, Replacement, Rechargeable
510(k) Number K980224
Device Name ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822
Applicant
Alexander Mfg. Co.
1511 S Garfield Pl.
Mason City,  IA  50401
Applicant Contact KEN HEIMENDINGER
Correspondent
Alexander Mfg. Co.
1511 S Garfield Pl.
Mason City,  IA  50401
Correspondent Contact KEN HEIMENDINGER
Regulation Number878.4820
Classification Product Code
MOQ  
Date Received01/22/1998
Decision Date 04/02/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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