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PRECISION GAS MIXER

K781417 Class I Traditional
Decision Date
1978-09-20
Sponsor / Applicant
Medicor USA , Ltd.

Technical Specification

510(k) Submission ID K781417
Product Code LCH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1978-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRECISION GAS MIXER received FDA 510(k) clearance under submission number K781417, sponsored by Medicor USA , Ltd.. 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 1978-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code LCH and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.