DeviceClearance

OPTUM, INTRAORAL CAMERA SYSTEM— 510(k) K983739

Substantially Equivalent

Camsight, Inc.

FDA 510(k) clearance K983739 for OPTUM, INTRAORAL CAMERA SYSTEM, Substantially Equivalent on 1999-01-19. Applicant: Camsight, Inc.. Device class: 1.

Clearance details

Applicant
Camsight, Inc.
Product code
Code EIA
Device class
Class 1
Regulation
21 CFR 872.6640
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Los Angeles, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code EIA

view all

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