NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER— 510(k) K042484

Name: FDA 510(k) clearance K042484
Creator: U.S. Food and Drug Administration
Published: 2004-10-20

Substantially Equivalent

Nai Technology Products

FDA 510(k) clearance K042484 for NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER, Substantially Equivalent on 2004-10-20. Applicant: Nai Technology Products. Device class: 2.

Clearance details

Applicant: Nai Technology Products
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 2004-09-13
Decision date: 2004-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Upland, CA, US

Download summary PDF View on FDA.gov ↗

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