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DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER

K932430 Class II Traditional
Decision Date
1994-05-02
Sponsor / Applicant
Pharmacia Deltec, Inc.

Technical Specification

510(k) Submission ID K932430
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 1994-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER received FDA 510(k) clearance under submission number K932430, sponsored by Pharmacia Deltec, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1994-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.