Altomed Malhotra Platinum Segments— 510(k) K170591

Name: FDA 510(k) clearance K170591
Creator: U.S. Food and Drug Administration
Published: 2017-06-06

Substantially Equivalent

Altomed Limited

FDA 510(k) clearance K170591 for Altomed Malhotra Platinum Segments, Substantially Equivalent on 2017-06-06. Applicant: Altomed Limited. Device class: 2.

Clearance details

Applicant: Altomed Limited
Product code: Code MML
Device class: Class 2
Regulation: 21 CFR 886.5700
Advisory panel: Ophthalmic
Date received: 2017-02-28
Decision date: 2017-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bolden, Tyne And Wear, GB

Download summary PDF View on FDA.gov ↗

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