meddevicedb.com FDA Device Reference

ACACIAS PHARM/PUMP

K912771 Class II Traditional
Decision Date
1992-02-14
Sponsor / Applicant
Acacia, Inc.

Technical Specification

510(k) Submission ID K912771
Product Code LHI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1992-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACACIAS PHARM/PUMP received FDA 510(k) clearance under submission number K912771, sponsored by Acacia, Inc.. 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 1992-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code LHI and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.