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SECQUIRE CELL SEPARATOR

K024080 Class I Traditional
Decision Date
2003-07-02
Sponsor / Applicant
Perfusion Partners & Assoc., Inc.

Technical Specification

510(k) Submission ID K024080
Product Code JQC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2050
Decision Date 2003-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECQUIRE CELL SEPARATOR received FDA 510(k) clearance under submission number K024080, sponsored by Perfusion Partners & Assoc., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2003-07-02.

Classification & Regulation

This clearance is catalogued under FDA product code JQC and 21 CFR 862.2050, within the Clinical Chemistry review panel as a Class I device.