meddevicedb.com FDA Device Reference

PEDIATRIC INGESTASCAN

K003305 Class II Traditional
Decision Date
2000-12-22
Sponsor / Applicant
Adams Electronics, Inc.

Technical Specification

510(k) Submission ID K003305
Product Code HPM
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4400
Decision Date 2000-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PEDIATRIC INGESTASCAN received FDA 510(k) clearance under submission number K003305, sponsored by Adams Electronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code HPM and 21 CFR 886.4400, within the Ophthalmic review panel as a Class II device.