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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Powered
510(k) Number K952355
Device Name THE HILL ADJUSTABLE 90MD
Applicant
Hill Laboratories Co.
445 Lincoln Hwy.
Malvern,  PA  19355
Applicant Contact HOWARD A HILL
Correspondent
Hill Laboratories Co.
445 Lincoln Hwy.
Malvern,  PA  19355
Correspondent Contact HOWARD A HILL
Regulation Number890.3760
Classification Product Code
INQ  
Date Received04/27/1995
Decision Date 06/22/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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