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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Flask, Tissue Culture
510(k) Number K873889
Device Name TISSUE CULTURE TUBES
Applicant
Nunc, Inc.
Attorney At Law
2085 Rustin Ave.
Riverside,  CA  92507
Applicant Contact STANLEY E FRY
Correspondent
Nunc, Inc.
Attorney At Law
2085 Rustin Ave.
Riverside,  CA  92507
Correspondent Contact STANLEY E FRY
Regulation Number864.2240
Classification Product Code
KJA  
Date Received09/23/1987
Decision Date 11/25/1987
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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