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CHARTERMED TPN-EVA BAGS

K973103 Class II Traditional
Decision Date
1997-11-24
Sponsor / Applicant
Chartermed, Inc.

Technical Specification

510(k) Submission ID K973103
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 1997-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHARTERMED TPN-EVA BAGS received FDA 510(k) clearance under submission number K973103, sponsored by Chartermed, 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 1997-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code KPE and 21 CFR 880.5025, within the General Hospital review panel as a Class II device.