MARCO STANDARD LENSMETERS 101,201— 510(k) K930441

Name: FDA 510(k) clearance K930441
Creator: U.S. Food and Drug Administration
Published: 1993-07-06

Substantially Equivalent

Marco Ophthalmic, Inc.

FDA 510(k) clearance K930441 for MARCO STANDARD LENSMETERS 101,201, Substantially Equivalent on 1993-07-06. Applicant: Marco Ophthalmic, Inc.. Device class: 1.

Clearance details

Applicant: Marco Ophthalmic, Inc.
Product code: Code HLM
Device class: Class 1
Regulation: 21 CFR 886.1425
Advisory panel: Ophthalmic
Date received: 1993-01-26
Decision date: 1993-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLM

view all

K944022 — LENSCHEK1994-11-17
K940997 — AL-33001994-09-29
K936199 — AUTOMATIC LENSOMETER1994-09-28
K930445 — MARCO LM-770 DIGITAL PROJECTION LENSMETER1993-06-21
K924776 — BURTON LENSMETER - MODEL 20211993-04-05

More clearances from Marco Ophthalmic, Inc.

view all

K943234 — MS-30 AUTOMATIC PERIMETER1994-07-27
K930437 — MARCO STANDARD RADIUSGAUGES1993-08-09
K930438 — MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPS1993-08-09
K930442 — MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPS1993-08-09
K930444 — MARCO STANDARD KERATOMETERS1993-08-09

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