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CRYOCHECK PREKALLIKREIN DEFICIENT PLALSMA, MODEL FDPK10/10 (10 X 1.0 ML), FDPK10/25 (25 X 1.0ML)

K990296 Class II Traditional
Decision Date
1999-03-18
Sponsor / Applicant
Precision Biologic

Technical Specification

510(k) Submission ID K990296
Product Code GJT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7290
Decision Date 1999-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRYOCHECK PREKALLIKREIN DEFICIENT PLALSMA, MODEL FDPK10/10 (10 X 1.0 ML), FDPK10/25 (25 X 1.0ML) received FDA 510(k) clearance under submission number K990296, sponsored by Precision Biologic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1999-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code GJT and 21 CFR 864.7290, within the Hematology review panel as a Class II device.