NIDEK LM-870 AUTOMATIC LENSMETER— 510(k) K884188

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K884188 for NIDEK LM-870 AUTOMATIC LENSMETER, Substantially Equivalent on 1988-11-23. Applicant: Nidek, Inc.. Device class: 1.

Clearance details

Applicant: Nidek, Inc.
Product code: Code HLM
Device class: Class 1
Regulation: 21 CFR 886.1425
Advisory panel: Ophthalmic
Date received: 1988-10-05
Decision date: 1988-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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K930445 — MARCO LM-770 DIGITAL PROJECTION LENSMETER1993-06-21

More clearances from Nidek, Inc.

K050336 — OPD-STATION SOFTWARE2005-08-24
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K032085 — GREEN LASER PHOTOCOAGULATOR MODEL GYC-10002003-10-03
K013694 — NIDEK ADVANCED VISION INFORMATION SYSTEM (NAVIS)2002-11-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.