meddevicedb.com FDA Device Reference

DUPONT PREP FOUR-SOLVENT RETROFIT KIT

K851393 Class I Traditional
Decision Date
1985-07-12
Sponsor / Applicant
E.I. Dupont DE Nemours & Co., Inc.

Technical Specification

510(k) Submission ID K851393
Product Code JJH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2310
Decision Date 1985-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUPONT PREP FOUR-SOLVENT RETROFIT KIT received FDA 510(k) clearance under submission number K851393, sponsored by E.I. Dupont DE Nemours & Co., 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 1985-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code JJH and 21 CFR 862.2310, within the Clinical Chemistry review panel as a Class I device.