meddevicedb.com FDA Device Reference

SERUM FREE TISSUE CULTURE MEDIA

K803041 Class I Traditional
Decision Date
1980-12-30
Sponsor / Applicant
Cartaya Assoc.

Technical Specification

510(k) Submission ID K803041
Product Code KIT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.2220
Decision Date 1980-12-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERUM FREE TISSUE CULTURE MEDIA received FDA 510(k) clearance under submission number K803041, sponsored by Cartaya Assoc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-12-30.

Classification & Regulation

This clearance is catalogued under FDA product code KIT and 21 CFR 864.2220, within the Hematology review panel as a Class I device.