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HydroPearl Microspheres, HydroPearl Microspheres

K150870 Class II Traditional
Decision Date
2015-12-21
Sponsor / Applicant
MicroVention, Inc.

Technical Specification

510(k) Submission ID K150870
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2015-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HydroPearl Microspheres, HydroPearl Microspheres received FDA 510(k) clearance under submission number K150870, sponsored by MicroVention, 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 2015-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.