meddevicedb.com FDA Device Reference

PACH-PEN CALCULATOR

K884619 Class II Traditional
Decision Date
1989-02-02
Sponsor / Applicant
Oculab, Inc.

Technical Specification

510(k) Submission ID K884619
Product Code DXG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1435
Decision Date 1989-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACH-PEN CALCULATOR received FDA 510(k) clearance under submission number K884619, sponsored by Oculab, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-02-02.

Classification & Regulation

This clearance is catalogued under FDA product code DXG and 21 CFR 870.1435, within the Cardiovascular review panel as a Class II device.