RODENSTOCK SLITLAMP (MODEL 5000 & 4000)— 510(k) K962532

Name: FDA 510(k) clearance K962532
Creator: U.S. Food and Drug Administration
Published: 1996-07-25

Substantially Equivalent

Expertech Assoc., Inc.

FDA 510(k) clearance K962532 for RODENSTOCK SLITLAMP (MODEL 5000 & 4000), Substantially Equivalent on 1996-07-25. Applicant: Expertech Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Expertech Assoc., Inc.
Product code: Code HJO
Device class: Class 2
Regulation: 21 CFR 886.1850
Advisory panel: Ophthalmic
Date received: 1996-06-28
Decision date: 1996-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, MA, US

Download summary PDF View on FDA.gov ↗

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