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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Media And Components, Synthetic Cell And Tissue Culture
510(k) Number K860282
Device Name RPMI 1640 W/GLUTAMINE W/HEPES
Applicant
Newport Biosystems, Inc.
Rod Roberts
150 E. Edinger, Suite C
Santa Ana,  CA  92705
Applicant Contact CULT INNOV
Correspondent
Newport Biosystems, Inc.
Rod Roberts
150 E. Edinger, Suite C
Santa Ana,  CA  92705
Correspondent Contact CULT INNOV
Regulation Number864.2220
Classification Product Code
KIT  
Date Received01/28/1986
Decision Date 02/05/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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