meddevicedb.com FDA Device Reference

MINISCOPE MS-2

K830411 Class II Traditional
Decision Date
1983-04-27
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K830411
Product Code DSP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3535
Decision Date 1983-04-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINISCOPE MS-2 received FDA 510(k) clearance under submission number K830411, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1983-04-27.

Classification & Regulation

This clearance is catalogued under FDA product code DSP and 21 CFR 870.3535, within the Cardiovascular review panel as a Class II device.