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SCIMED OPTAMUM OPER PERIPHERAL ANGIOPLASTY CATH

K910155 Class II Traditional
Decision Date
1991-02-07
Sponsor / Applicant
Scimed Life Systems, Inc.

Technical Specification

510(k) Submission ID K910155
Product Code LIT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 1991-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCIMED OPTAMUM OPER PERIPHERAL ANGIOPLASTY CATH received FDA 510(k) clearance under submission number K910155, sponsored by Scimed Life Systems, 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 1991-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code LIT and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.