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MULTIWASH

K813426 Class I Traditional
Decision Date
1981-12-22
Sponsor / Applicant
Flow Laboratories, Inc.

Technical Specification

510(k) Submission ID K813426
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1981-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIWASH received FDA 510(k) clearance under submission number K813426, sponsored by Flow Laboratories, 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 1981-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.