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InVision™ 1.5 Surgical Theatre

K240157 Class II Traditional
Decision Date
2024-02-15
Sponsor / Applicant
Deerfield Imaging, Inc.

Technical Specification

510(k) Submission ID K240157
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2024-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

InVision™ 1.5 Surgical Theatre received FDA 510(k) clearance under submission number K240157, sponsored by Deerfield Imaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-02-15.

Classification & Regulation

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