MAXICAMERA II— 510(k) K770343

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K770343 for MAXICAMERA II, Substantially Equivalent on 1977-02-28. 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: 1977-02-18
Decision date: 1977-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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