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COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG

K831888 Class I Traditional
Decision Date
1983-07-12
Sponsor / Applicant
Portable Travtion Device Co.

Technical Specification

510(k) Submission ID K831888
Product Code HST
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5850
Decision Date 1983-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPUTERIZED TOMOGRAPHY-HYPERBARIC OXYG received FDA 510(k) clearance under submission number K831888, sponsored by Portable Travtion Device Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1983-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code HST and 21 CFR 888.5850, within the Orthopedic review panel as a Class I device.