meddevicedb.com FDA Device Reference

IV COMFORT PAD

K930663 Class I Traditional
Decision Date
1993-09-30
Sponsor / Applicant
D.J. Scott Mfg., Inc.

Technical Specification

510(k) Submission ID K930663
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1993-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV COMFORT PAD received FDA 510(k) clearance under submission number K930663, sponsored by D.J. Scott Mfg., 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 1993-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code KMK and 21 CFR 880.5210, within the General Hospital review panel as a Class I device.