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QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE

K030721 Class II Special
Decision Date
2003-03-31
Sponsor / Applicant
Ballard Medical Products

Technical Specification

510(k) Submission ID K030721
Product Code LRO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2003-03-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE received FDA 510(k) clearance under submission number K030721, sponsored by Ballard Medical Products. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code LRO and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.