meddevicedb.com FDA Device Reference

WESCOR 5500 VAPOR PRESSURE OSMOMETER

K834214 Class I Traditional
Decision Date
1984-03-30
Sponsor / Applicant
Wescor, Inc.

Technical Specification

510(k) Submission ID K834214
Product Code JJM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2730
Decision Date 1984-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WESCOR 5500 VAPOR PRESSURE OSMOMETER received FDA 510(k) clearance under submission number K834214, sponsored by Wescor, 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 1984-03-30.

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.