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NEUROVASCULAR ARRAY COIL, MODEL NVA-127-16-A

K052497 Class II Special
Decision Date
2005-10-12
Sponsor / Applicant
Invivo Corp.

Technical Specification

510(k) Submission ID K052497
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2005-10-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROVASCULAR ARRAY COIL, MODEL NVA-127-16-A received FDA 510(k) clearance under submission number K052497, sponsored by Invivo Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-10-12.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.