TURBOTRON 20/20— 510(k) K902920

Name: FDA 510(k) clearance K902920
Creator: U.S. Food and Drug Administration
Published: 1991-10-10

Substantially Equivalent

Prestige Manufacturing Snd Bhd

FDA 510(k) clearance K902920 for TURBOTRON 20/20, Substantially Equivalent on 1991-10-10. Applicant: Prestige Manufacturing Snd Bhd. Device class: 2.

Clearance details

Applicant: Prestige Manufacturing Snd Bhd
Product code: Code LYL
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1990-07-03
Decision date: 1991-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Campbell, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LYL

product code LYL

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.