LM-850 AUTOMATIC LENSMETER— 510(k) K861064

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K861064 for LM-850 AUTOMATIC LENSMETER, Substantially Equivalent on 1986-04-15. 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: 1986-03-20
Decision date: 1986-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLM

K944022 — LENSCHEK1994-11-17
K940997 — AL-33001994-09-29
K936199 — AUTOMATIC LENSOMETER1994-09-28
K930441 — MARCO STANDARD LENSMETERS 101,2011993-07-06
K930445 — MARCO LM-770 DIGITAL PROJECTION LENSMETER1993-06-21

More clearances from Nidek, Inc.

K050336 — OPD-STATION SOFTWARE2005-08-24
K042785 — MULTI COLOR LASER PHOTOCOAGULATOR, MODEL MC-3002004-12-14
K031733 — NON-CONTACT TONOMETER, MODEL NT-40002003-12-04
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.