MODIFIED CLINICAL WIDEFIELD SPECULAR MICROSCOPE 50— 510(k) K854440

Name: FDA 510(k) clearance K854440
Creator: U.S. Food and Drug Administration
Published: 1985-12-16

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K854440 for MODIFIED CLINICAL WIDEFIELD SPECULAR MICROSCOPE 50, Substantially Equivalent on 1985-12-16. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HRM
Device class: Class 1
Regulation: 21 CFR 878.4700
Advisory panel: General, Plastic Surgery
Date received: 1985-11-05
Decision date: 1985-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HRM

view all

K932720 — HM-09701993-09-07
K930439 — MARCO SURGISCOPE OPERATION MICROSCOPES1993-07-22
K920641 — ALCON OPERATING MICROSCOPES1992-10-09
K914956 — KEELER KONAN SPECULAR MICROSCOPE SP55001992-02-03
K891584 — S 22 INSTRUMENT STAND1989-06-08

More clearances from Keeler Instruments, Inc.

view all

K181143 — Keeler TonoCare Tonometer2019-02-08
K112093 — CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER2011-12-08
K093298 — PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-20002010-12-10
K100500 — PSL CLASSIC SLIT LAMP2010-03-09
K062412 — CRYOMATIC2006-11-06

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