
Popper & Sons, Inc.
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J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI is an FDA 510(k)-cleared medical device (K843830) manufactured by Popper & Sons, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 25, 1984. Regulation: 8.