meddevicedb.com FDA Device Reference

I.S.M. PRODUCT FAMILY MODEL P2400C,A & ABC

K854171 Class II Traditional
Decision Date
1985-11-06
Sponsor / Applicant
Intl. Solarium Manufacturer, Inc.

Technical Specification

510(k) Submission ID K854171
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1985-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I.S.M. PRODUCT FAMILY MODEL P2400C,A & ABC received FDA 510(k) clearance under submission number K854171, sponsored by Intl. Solarium Manufacturer, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1985-11-06.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.