ULTRASONIC PACHYMETER— 510(k) K921705

Substantially Equivalent

Precision Corneal Instruments

FDA 510(k) clearance K921705 for ULTRASONIC PACHYMETER, Substantially Equivalent on 1992-11-16. Applicant: Precision Corneal Instruments.

Clearance details

Applicant: Precision Corneal Instruments
Product code: Code IYO
Advisory panel: Radiology
Date received: 1992-04-10
Decision date: 1992-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Gatos, CA, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.