SPECTRA VU 1000 SERIES INTRAORAL CAMERA, SPECTRA VU 2000 SERIES INTRAORAL CAMERA, SPECTRA VU HDDI SV I INTRAORAL CAMERA,— 510(k) K984332

Name: FDA 510(k) clearance K984332
Creator: U.S. Food and Drug Administration
Published: 1999-04-29

Substantially Equivalent

International Technology Concepts

FDA 510(k) clearance K984332 for SPECTRA VU 1000 SERIES INTRAORAL CAMERA, SPECTRA VU 2000 SERIES INTRAORAL CAMERA, SPECTRA VU HDDI SV I INTRAORAL CAMERA,, Substantially Equivalent on 1999-04-29. Applicant: International Technology Concepts. Device class: 1.

Clearance details

Applicant: International Technology Concepts
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1998-12-03
Decision date: 1999-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, 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.