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ISLAM BONE MARROW BIOPSY NEEDLE

K820339 Class I Traditional
Decision Date
1982-02-23
Sponsor / Applicant
Downs Surgical , Ltd.

Technical Specification

510(k) Submission ID K820339
Product Code GDM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1982-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISLAM BONE MARROW BIOPSY NEEDLE received FDA 510(k) clearance under submission number K820339, sponsored by Downs Surgical , Ltd.. 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 1982-02-23.

Classification & Regulation

This clearance is catalogued under FDA product code GDM and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.