meddevicedb.com FDA Device Reference

ACTION PAC

K851276 Traditional
Decision Date
1985-05-15
Sponsor / Applicant
South Mountain Medical

Technical Specification

510(k) Submission ID K851276
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1985-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTION PAC received FDA 510(k) clearance under submission number K851276, sponsored by South Mountain Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1985-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.