CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)— 510(k) K000637

Name: FDA 510(k) clearance K000637
Creator: U.S. Food and Drug Administration
Published: 2000-05-19

Unknown

Alcon Laboratories, Inc.

FDA 510(k) clearance K000637 for CUSTOMCORNEA MEASUREMENT DEVICE (CCMD), Unknown on 2000-05-19. Applicant: Alcon Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Alcon Laboratories, Inc.
Product code: Code NCF
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 2000-02-25
Decision date: 2000-05-19
Decision: Unknown
Clearance type: Traditional
Location: Orlando, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NCF

product code NCF

Injury: 129
Total: 129

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.