CONMED LINVATEC INSTRUMENT STERILIZATION TRAY— 510(k) K052992

Name: FDA 510(k) clearance K052992
Creator: U.S. Food and Drug Administration
Published: 2006-10-16

Substantially Equivalent

Conmed Linvatec

FDA 510(k) clearance K052992 for CONMED LINVATEC INSTRUMENT STERILIZATION TRAY, Substantially Equivalent on 2006-10-16. Applicant: Conmed Linvatec. Device class: 2.

Clearance details

Applicant: Conmed Linvatec
Product code: Code FRG
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2005-10-25
Decision date: 2006-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

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.