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SYSTEM CONTROLLER 720 SERIES

K791661 Class I Traditional
Decision Date
1979-09-24
Sponsor / Applicant
Waters Assoc., Inc.

Technical Specification

510(k) Submission ID K791661
Product Code KIE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1979-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEM CONTROLLER 720 SERIES received FDA 510(k) clearance under submission number K791661, sponsored by Waters Assoc., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1979-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code KIE and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.