VIDEO PLUS SYSTEM, SERIES 95000— 510(k) K992666

Name: FDA 510(k) clearance K992666
Creator: U.S. Food and Drug Administration
Published: 1999-10-13

Substantially Equivalent

Camtronics, Ltd.

FDA 510(k) clearance K992666 for VIDEO PLUS SYSTEM, SERIES 95000, Substantially Equivalent on 1999-10-13. Applicant: Camtronics, Ltd.. Device class: 2.

Clearance details

Applicant: Camtronics, Ltd.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 1999-08-09
Decision date: 1999-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hartland, WI, US

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Recent devices under product code LLZ

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More clearances from Camtronics, Ltd.

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K021236 — SURGERY AND ACCESSORIES2002-07-17
K013032 — PHYSIOLOG, SERIES 950002002-06-04
K992259 — ECHOCARDIOGRAPHY SYSTEM SERIES 950001999-09-08
K990066 — CCD CAMERA, MODEL 90001999-03-17
K955519 — ANALYTICAL REVIEW STATION1996-05-09

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.