ALM ILLUMINATOR SERIES LIGHT SYSTEM— 510(k) K922409

Name: FDA 510(k) clearance K922409
Creator: U.S. Food and Drug Administration
Published: 1993-01-12

Substantially Equivalent

Alm Surgical Equipment, Inc.

FDA 510(k) clearance K922409 for ALM ILLUMINATOR SERIES LIGHT SYSTEM, Substantially Equivalent on 1993-01-12. Applicant: Alm Surgical Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Alm Surgical Equipment, Inc.
Product code: Code FSQ
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1992-05-21
Decision date: 1993-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FSQ

view all

K930686 — MIDMARK SURGICAL LIGHTING SYSTEMS1993-07-30
K932139 — LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT1993-07-30
K921848 — BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHT1992-10-01
K803067 — SURG-FLEX 10 LIGHT1981-02-26
K810018 — SURG-FLEX 5 SURGICAL LIGHT1981-01-23

More clearances from Alm Surgical Equipment, Inc.

view all

K982063 — ALM PRISMALIX (PRX) SURGICAL LIGHT1998-09-22
K961886 — DRAGER GEMINA WALL-MOUNTED WORKPLACE1996-07-30
K961742 — DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEM1996-07-26
K945102 — MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE1994-11-04
K942043 — DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032E1994-07-13

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