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NAC PLUS NEEDLELESS ACCESS CONNECTOR

K011193 Class II Traditional
Decision Date
2001-06-12
Sponsor / Applicant
Porex Medical Products

Technical Specification

510(k) Submission ID K011193
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2001-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NAC PLUS NEEDLELESS ACCESS CONNECTOR received FDA 510(k) clearance under submission number K011193, sponsored by Porex Medical Products. 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 2001-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.