(MICRO-KERATRON, MICRO DUCT TREPHINE)— 510(k) K791763

Name: FDA 510(k) clearance K791763
Creator: U.S. Food and Drug Administration
Published: 1979-11-05

Substantially Equivalent

Intl. Ophthalmic Industries Corp.

FDA 510(k) clearance K791763 for (MICRO-KERATRON, MICRO DUCT TREPHINE), Substantially Equivalent on 1979-11-05. Applicant: Intl. Ophthalmic Industries Corp.. Device class: 1.

Clearance details

Applicant: Intl. Ophthalmic Industries Corp.
Product code: Code HRG
Device class: Class 1
Regulation: 21 CFR 886.4070
Advisory panel: Ophthalmic
Date received: 1979-09-05
Decision date: 1979-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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