meddevicedb.com FDA Device Reference

RECAP

K780665 Class II Traditional
Decision Date
1978-06-06
Sponsor / Applicant
Bca Biological Corp. of America

Technical Specification

510(k) Submission ID K780665
Product Code KSF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9650
Decision Date 1978-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECAP received FDA 510(k) clearance under submission number K780665, sponsored by Bca Biological Corp. of America. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1978-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code KSF and 21 CFR 864.9650, within the Hematology review panel as a Class II device.