meddevicedb.com FDA Device Reference

MODEL 902 STAND

K780759 Class I Traditional
Decision Date
1978-05-19
Sponsor / Applicant
Applied Medical Research

Technical Specification

510(k) Submission ID K780759
Product Code FSH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1978-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 902 STAND received FDA 510(k) clearance under submission number K780759, sponsored by Applied Medical Research. 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 1978-05-19.

Classification & Regulation

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