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OCS Heart Leukocyte Depleting Filter

K231362 Class II Traditional
Decision Date
2023-10-31
Sponsor / Applicant
TransMedics, Inc.

Technical Specification

510(k) Submission ID K231362
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 2023-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OCS Heart Leukocyte Depleting Filter received FDA 510(k) clearance under submission number K231362, sponsored by TransMedics, 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 2023-10-31.

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.