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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Aspiration And Injection, Reusable
510(k) Number K843830
Device Name J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI
Applicant
POPPER & SONS, INC.
300 DENTON AVE.
NEW HYDE PARK,  NY  11040
Applicant Contact ROBERT A POPPER
Correspondent
POPPER & SONS, INC.
300 DENTON AVE.
NEW HYDE PARK,  NY  11040
Correspondent Contact ROBERT A POPPER
Regulation Number878.4800
Classification Product Code
GDM  
Date Received10/01/1984
Decision Date 10/26/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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