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ACA ACTIVATED PARTIAL THROMBOPLASTIN TIME ANALYTIC

K851126 Class II Traditional
Decision Date
1985-05-29
Sponsor / Applicant
E.I. Dupont DE Nemours & Co., Inc.

Technical Specification

510(k) Submission ID K851126
Product Code GGW
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7925
Decision Date 1985-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACA ACTIVATED PARTIAL THROMBOPLASTIN TIME ANALYTIC received FDA 510(k) clearance under submission number K851126, sponsored by E.I. Dupont DE Nemours & Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1985-05-29.

Classification & Regulation

This clearance is catalogued under FDA product code GGW and 21 CFR 864.7925, within the Hematology review panel as a Class II device.