XPERT NCT— 510(k) K941865

Name: FDA 510(k) clearance K941865
Creator: U.S. Food and Drug Administration
Published: 1994-09-29

Substantially Equivalent

Reichert Ophthalmic Instruments, Div. Leica, Inc.

FDA 510(k) clearance K941865 for XPERT NCT, Substantially Equivalent on 1994-09-29. Applicant: Reichert Ophthalmic Instruments, Div. Leica, Inc.. Device class: 2.

Clearance details

Applicant: Reichert Ophthalmic Instruments, Div. Leica, Inc.
Product code: Code HKX
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 1994-04-18
Decision date: 1994-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Depew, NY, US

Download summary PDF View on FDA.gov ↗

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