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CORVAC BLOOD COLLECTION TUBE

K915213 Class II Traditional
Decision Date
1992-01-08
Sponsor / Applicant
Sherwood Medical Co.

Technical Specification

510(k) Submission ID K915213
Product Code GIM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1992-01-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORVAC BLOOD COLLECTION TUBE received FDA 510(k) clearance under submission number K915213, sponsored by Sherwood Medical Co.. 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 1992-01-08.

Classification & Regulation

This clearance is catalogued under FDA product code GIM and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.