meddevicedb.com FDA Device Reference

CPR GENERAL SURGERY TRAY

K960241 Class II Traditional
Decision Date
1996-03-22
Sponsor / Applicant
Custom Pack Reliability

Technical Specification

510(k) Submission ID K960241
Product Code LWI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1996-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CPR GENERAL SURGERY TRAY received FDA 510(k) clearance under submission number K960241, sponsored by Custom Pack Reliability. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code LWI and 21 CFR 892.1560, within the Radiology review panel as a Class II device.