Clearance Summary
GARDNER TYPE BONE MARROW NEEDLE received FDA 510(k) clearance under submission number K841301, sponsored by Popper & Sons, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1984-06-05.
- Submission: K841301
- Applicant / Sponsor: Popper & Sons, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1984-06-05
Classification & Regulation
This clearance is catalogued under FDA product code GAA and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.