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PACIFIC HEMOSTASIS INR CONTROL PLASMAS, MODEL CATALOG 100560

K010750 Class II Traditional
Decision Date
2001-09-07
Sponsor / Applicant
Fisher Diagnostics

Technical Specification

510(k) Submission ID K010750
Product Code GGN
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 2001-09-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACIFIC HEMOSTASIS INR CONTROL PLASMAS, MODEL CATALOG 100560 received FDA 510(k) clearance under submission number K010750, sponsored by Fisher Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2001-09-07.

Classification & Regulation

This clearance is catalogued under FDA product code GGN and 21 CFR 864.5425, within the Hematology review panel as a Class II device.