KELLER CEPHALOMETRIC DEVICE— 510(k) K850197

Substantially Equivalent

Gary D. Keller

FDA 510(k) clearance K850197 for KELLER CEPHALOMETRIC DEVICE, Substantially Equivalent on 1985-03-22. Applicant: Gary D. Keller. Device class: 1.

Clearance details

Applicant: Gary D. Keller
Product code: Code IWY
Device class: Class 1
Regulation: 21 CFR 892.1920
Advisory panel: Radiology
Date received: 1985-01-18
Decision date: 1985-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sherman, TX, US

Download summary PDF View on FDA.gov ↗

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K864527 — DUOCEPH1987-01-07
K844549 — HEAD-SPINE STABILIZER HSS-11985-03-01

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