VenusCT— 510(k) K260510

Substantially Equivalent

Linatech, LLC

FDA 510(k) clearance K260510 for VenusCT, Substantially Equivalent on 2026-10-19. Applicant: Linatech, LLC. Device class: 2.

Clearance details

Applicant: Linatech, LLC
Product code: Product code SFV
Device class: Class 2
Regulation: 21 CFR 892.1750
Advisory panel: Radiology
Date received: 2026-02-17
Decision date: 2026-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code SFV

K250318 — Planmed XFI2025-09-26

More clearances from Linatech, LLC

K232489 — VenusX2024-04-12
K092550 — TIGRT IVS2009-12-15
K090893 — TIGRT TPS2009-07-15
K090802 — TIGRT MLC, TIGRT DMLC2009-07-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.