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INTERSEPT PEDIACTRIC EXTRACORPOREAL FILT

K823108 Class II Traditional
Decision Date
1982-11-30
Sponsor / Applicant
Extracorporeal Medical Specialities, Inc.

Technical Specification

510(k) Submission ID K823108
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 1982-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERSEPT PEDIACTRIC EXTRACORPOREAL FILT received FDA 510(k) clearance under submission number K823108, sponsored by Extracorporeal Medical Specialities, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code DTM and 21 CFR 870.4260, within the Cardiovascular review panel as a Class II device.