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OSMOMETER MODEL OM-6010

K811179 Class I Traditional
Decision Date
1981-05-15
Sponsor / Applicant
Fiske Med Science

Technical Specification

510(k) Submission ID K811179
Product Code JJM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2730
Decision Date 1981-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSMOMETER MODEL OM-6010 received FDA 510(k) clearance under submission number K811179, sponsored by Fiske Med Science. 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 1981-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code JJM and 21 CFR 862.2730, within the Clinical Chemistry review panel as a Class I device.