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PACIFIC HEMOSTASIS THROMBOSCREEN 400C

K992130 Class II Traditional
Decision Date
1999-09-03
Sponsor / Applicant
Pacific Hemostasis

Technical Specification

510(k) Submission ID K992130
Product Code KQG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1999-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACIFIC HEMOSTASIS THROMBOSCREEN 400C received FDA 510(k) clearance under submission number K992130, 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 1999-09-03.

Classification & Regulation

This clearance is catalogued under FDA product code KQG and 21 CFR 864.5400, within the Hematology review panel as a Class II device.