DOHLMAN DOANE KERATOPROTHESIS— 510(k) K915062

Name: FDA 510(k) clearance K915062
Creator: U.S. Food and Drug Administration
Published: 1992-01-21

Substantially Equivalent

Mackeen Consultants, Ltd.

FDA 510(k) clearance K915062 for DOHLMAN DOANE KERATOPROTHESIS, Substantially Equivalent on 1992-01-21. Applicant: Mackeen Consultants, Ltd.. Device class: 2.

Clearance details

Applicant: Mackeen Consultants, Ltd.
Product code: Code HQM
Device class: Class 2
Regulation: 21 CFR 886.3400
Advisory panel: Ophthalmic
Date received: 1991-11-08
Decision date: 1992-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQM

view all

K182986 — Boston Keratoprosthesis, Type I Lucia2019-01-30
K121203 — BOSTON KERATOPROSTHESIS OR BOSTON KPRO2013-05-10
K013756 — ALPHACOR; ALPHACOR-A (FOR AHAKIC EYES); ALPHACOR-P (FOR PHAKIC OR PSEUDOPHAKIC EYES)2002-08-29

More clearances from Mackeen Consultants, Ltd.

view all

K852737 — LACTOPLATE1985-10-25

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