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SAFETY SUBCUTANEOUS TISSUE INFUSION SET

K120195 Class II Traditional
Decision Date
2012-07-06
Sponsor / Applicant
Multi Med

Technical Specification

510(k) Submission ID K120195
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2012-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAFETY SUBCUTANEOUS TISSUE INFUSION SET received FDA 510(k) clearance under submission number K120195, sponsored by Multi Med. 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 2012-07-06.

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.