MAXI CAMERA/D— 510(k) K811676

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K811676 for MAXI CAMERA/D, Substantially Equivalent on 1981-07-02. Applicant: General Electric Co.. Device class: 1.

Clearance details

Applicant
General Electric Co.
Product code
Code IYX
Device class
Class 1
Regulation
21 CFR 892.1100
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code IYX

view all

More clearances from General Electric Co.

view all

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