MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL— 510(k) K791659

Name: FDA 510(k) clearance K791659
Creator: U.S. Food and Drug Administration
Published: 1979-10-11

Substantially Equivalent

Coburn Optical Ind., Inc.

FDA 510(k) clearance K791659 for MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL, Substantially Equivalent on 1979-10-11. Applicant: Coburn Optical Ind., Inc.. Device class: 2.

Clearance details

Applicant: Coburn Optical Ind., Inc.
Product code: Code HQF
Device class: Class 2
Regulation: 21 CFR 886.4390
Advisory panel: Ophthalmic
Date received: 1979-08-22
Decision date: 1979-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

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.