meddevicedb.com FDA Device Reference

RE-CELL SLIDE RECAP

K772139 Class II Traditional
Decision Date
1978-01-05
Sponsor / Applicant
Geometric Data, Div. Smithkline Corp.

Technical Specification

510(k) Submission ID K772139
Product Code JOY
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5260
Decision Date 1978-01-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RE-CELL SLIDE RECAP received FDA 510(k) clearance under submission number K772139, sponsored by Geometric Data, Div. Smithkline Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1978-01-05.

Classification & Regulation

This clearance is catalogued under FDA product code JOY and 21 CFR 864.5260, within the Hematology review panel as a Class II device.