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THROMBOSCREEN JOSHUA HEMOGLOBIN S SCREENING KIT

K872217 Class II Traditional
Decision Date
1987-07-31
Sponsor / Applicant
Pacific Hemostasis

Technical Specification

510(k) Submission ID K872217
Product Code GHM
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7825
Decision Date 1987-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THROMBOSCREEN JOSHUA HEMOGLOBIN S SCREENING KIT received FDA 510(k) clearance under submission number K872217, sponsored by Pacific Hemostasis. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1987-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code GHM and 21 CFR 864.7825, within the Hematology review panel as a Class II device.