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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 K924002
Device Name MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE
Applicant
Midland Mfg. Co.
55 Northern Blvd., Suite 301
Great Neck,  NY  11021
Applicant Contact ALLAN P SCHWARTZ
Correspondent
Midland Mfg. Co.
55 Northern Blvd., Suite 301
Great Neck,  NY  11021
Correspondent Contact ALLAN P SCHWARTZ
Regulation Number890.3760
Classification Product Code
INQ  
Date Received08/10/1992
Decision Date 11/09/1992
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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