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CORVAC PLASTIC BLOOD COLLECTION TUBE

K944814 Class II Traditional
Decision Date
1994-12-19
Sponsor / Applicant
Sherwood Medical Co.

Technical Specification

510(k) Submission ID K944814
Product Code GIM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1994-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORVAC PLASTIC BLOOD COLLECTION TUBE received FDA 510(k) clearance under submission number K944814, 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 1994-12-19.

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.