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SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL

K010598 Class II Traditional
Decision Date
2001-03-23
Sponsor / Applicant
Quantimetrix Corp.

Technical Specification

510(k) Submission ID K010598
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2001-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL received FDA 510(k) clearance under submission number K010598, sponsored by Quantimetrix Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2001-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.