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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Manual
510(k) Number K870310
Device Name VSID MEDICAL THREE-FOLDING BED
Applicant
China National Medicines & Health Prod. I/E Corp.
C/O Pacific Development Group
1000 T. Jefferson St. NW
Suite 500, Washington,  DC  20007
Applicant Contact LISA MITNICK
Correspondent
China National Medicines & Health Prod. I/E Corp.
C/O Pacific Development Group
1000 T. Jefferson St. NW
Suite 500, Washington,  DC  20007
Correspondent Contact LISA MITNICK
Regulation Number880.5120
Classification Product Code
FNJ  
Date Received01/28/1987
Decision Date 02/10/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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