DS ANTERIOR, DS BASE, DS HEAD-NECK, DS HEAD, FLEX (S,M,L)— 510(k) K123492

Name: FDA 510(k) clearance K123492
Creator: U.S. Food and Drug Administration
Published: 2012-12-13

Substantially Equivalent

Philips Medical Systems

FDA 510(k) clearance K123492 for DS ANTERIOR, DS BASE, DS HEAD-NECK, DS HEAD, FLEX (S,M,L), Substantially Equivalent on 2012-12-13. Applicant: Philips Medical Systems. Device class: 2.

Clearance details

Applicant: Philips Medical Systems
Product code: Code MOS
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 2012-11-13
Decision date: 2012-12-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Florida, FL, US

Download summary PDF View on FDA.gov ↗

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