meddevicedb.com FDA Device Reference

TISSUE CULTURE FLASK

K864021 Class I Traditional
Decision Date
1986-10-29
Sponsor / Applicant
Fenwal Laboratories

Technical Specification

510(k) Submission ID K864021
Product Code KJA
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.2240
Decision Date 1986-10-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE CULTURE FLASK received FDA 510(k) clearance under submission number K864021, sponsored by Fenwal Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1986-10-29.

Classification & Regulation

This clearance is catalogued under FDA product code KJA and 21 CFR 864.2240, within the Hematology review panel as a Class I device.