meddevicedb.com FDA Device Reference

CHROMATOGRAPHY KIT

K884176 Class I Traditional
Decision Date
1989-04-04
Sponsor / Applicant
Gelman Sciences, Inc.

Technical Specification

510(k) Submission ID K884176
Product Code DPA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2270
Decision Date 1989-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHROMATOGRAPHY KIT received FDA 510(k) clearance under submission number K884176, sponsored by Gelman Sciences, 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 1989-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code DPA and 21 CFR 862.2270, within the Clinical Chemistry review panel as a Class I device.