MID LABS TWIN ILLUMINATOR— 510(k) K932131

Name: FDA 510(k) clearance K932131
Creator: U.S. Food and Drug Administration
Published: 1994-04-01

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K932131 for MID LABS TWIN ILLUMINATOR, Substantially Equivalent on 1994-04-01. Applicant: Medical Instrument Development Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code EQH
Device class: Class 1
Regulation: 21 CFR 874.4350
Advisory panel: Ear, Nose, Throat
Date received: 1993-05-03
Decision date: 1994-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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