ALLEGRO VIEWING WAND— 510(k) K911783

Name: FDA 510(k) clearance K911783
Creator: U.S. Food and Drug Administration
Published: 1994-04-07

Substantially Equivalent

I.S.G. Technologies, Inc.

FDA 510(k) clearance K911783 for ALLEGRO VIEWING WAND, Substantially Equivalent on 1994-04-07. Applicant: I.S.G. Technologies, Inc.. Device class: 2.

Clearance details

Applicant: I.S.G. Technologies, Inc.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 1991-04-22
Decision date: 1994-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga Ontario, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLZ

view all

More clearances from I.S.G. Technologies, Inc.

view all

K993673 — SNN FLUORO NAVIGATION SYSTEM1999-12-21
K982570 — SNN SCOUT1999-01-13
K980684 — VR NETSERVE1998-05-06
K973413 — ID. STORE (RELEASE 2.0)1997-11-25
K970865 — ISG FAMILY OF VIEWING WANDS1997-06-04

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.