MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE— 510(k) K911901

Name: FDA 510(k) clearance K911901
Creator: U.S. Food and Drug Administration
Published: 1991-07-26

Substantially Equivalent

Stortz

FDA 510(k) clearance K911901 for MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE, Substantially Equivalent on 1991-07-26. Applicant: Stortz. Device class: 1.

Clearance details

Applicant: Stortz
Product code: Code ETF
Device class: Class 1
Regulation: 21 CFR 874.5300
Advisory panel: Ear, Nose, Throat
Date received: 1991-04-29
Decision date: 1991-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ETF

view all

K953457 — JEDMED SPECTRUM ENT CABINET1995-08-11
K945395 — PREMIER MIRROR WARMER1995-01-18
K932470 — LANGGASSE 901993-08-25
K910781 — #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES1991-05-15
K910243 — MOBILE TREATMENT CART1991-04-17

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