MULTI-FORMAT SFD MODEL 1720— 510(k) K800554

Name: FDA 510(k) clearance K800554
Creator: U.S. Food and Drug Administration
Published: 1980-04-10

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K800554 for MULTI-FORMAT SFD MODEL 1720, Substantially Equivalent on 1980-04-10. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code IXL
Device class: Class 2
Regulation: 21 CFR 892.1670
Advisory panel: Radiology
Date received: 1980-03-12
Decision date: 1980-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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