VIDEO FLUOROSCOPE— 510(k) K914414

Name: FDA 510(k) clearance K914414
Creator: U.S. Food and Drug Administration
Published: 1992-01-24

Substantially Equivalent

Raymax Medical Corp.

FDA 510(k) clearance K914414 for VIDEO FLUOROSCOPE, Substantially Equivalent on 1992-01-24. Applicant: Raymax Medical Corp.. Device class: 2.

Clearance details

Applicant: Raymax Medical Corp.
Product code: Code JAA
Device class: Class 2
Regulation: 21 CFR 892.1650
Advisory panel: Radiology
Date received: 1991-10-01
Decision date: 1992-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L4l 7k5, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAA

view all

K253103 — Nexus DRF Digital X-ray Imaging System2026-05-29
K251650 — Insight Enhanced DRF (EN-1002-01)2025-09-16
K242488 — Soteria E-View2025-01-06
K242948 — Adora DRFi (04550010)2024-12-23
K233380 — TRIDENT Mobile Fluoroscopy System2024-06-26

More clearances from Raymax Medical Corp.

view all

K930273 — ALPHA1993-07-13
K883431 — RAYMAX 2100 MODELS 2130 & 21361988-09-12

Adverse events under product code JAA

product code JAA

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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