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HEPARIN ACA ANALYTICAL TEST PACK

K843201 Class II Traditional
Decision Date
1984-11-30
Sponsor / Applicant
E.I. Dupont DE Nemours & Co., Inc.

Technical Specification

510(k) Submission ID K843201
Product Code KFF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7525
Decision Date 1984-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEPARIN ACA ANALYTICAL TEST PACK received FDA 510(k) clearance under submission number K843201, 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 1984-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code KFF and 21 CFR 864.7525, within the Hematology review panel as a Class II device.