meddevicedb.com FDA Device Reference

CUSTOM CV PACK

K936255 Class I Traditional
Decision Date
1994-03-31
Sponsor / Applicant
Associated Medical

Technical Specification

510(k) Submission ID K936255
Product Code KDD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1994-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUSTOM CV PACK received FDA 510(k) clearance under submission number K936255, sponsored by Associated Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1994-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code KDD and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.