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SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321

K991979 Class II Traditional
Decision Date
1999-09-03
Sponsor / Applicant
Medtronic Minimed

Technical Specification

510(k) Submission ID K991979
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1999-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 received FDA 510(k) clearance under submission number K991979, sponsored by Medtronic Minimed. 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 1999-09-03.

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.