meddevicedb.com FDA Device Reference

CRICKET

K955304 Class II Traditional
Decision Date
1996-05-16
Sponsor / Applicant
Microvena Corp.

Technical Specification

510(k) Submission ID K955304
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1996-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRICKET received FDA 510(k) clearance under submission number K955304, sponsored by Microvena Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1996-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.