meddevicedb.com FDA Device Reference

DOVER HYPERALIMENTATION DRESSING CHNG KT

K761099 Class I Traditional
Decision Date
1977-01-28
Sponsor / Applicant
Will Ross Co.

Technical Specification

510(k) Submission ID K761099
Product Code FRL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5300
Decision Date 1977-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOVER HYPERALIMENTATION DRESSING CHNG KT received FDA 510(k) clearance under submission number K761099, sponsored by Will Ross Co.. 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 1977-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code FRL and 21 CFR 880.5300, within the General Hospital review panel as a Class I device.