AUTOMATIC TRAY (ACT I & ACT II— 510(k) K820117

Name: FDA 510(k) clearance K820117
Creator: U.S. Food and Drug Administration
Published: 1982-02-18

Substantially Equivalent

Burbury & Cutter Ind., Inc.

FDA 510(k) clearance K820117 for AUTOMATIC TRAY (ACT I & ACT II, Substantially Equivalent on 1982-02-18. Applicant: Burbury & Cutter Ind., Inc.. Device class: 2.

Clearance details

Applicant: Burbury & Cutter Ind., Inc.
Product code: Code KPX
Device class: Class 2
Regulation: 21 CFR 892.1860
Advisory panel: Radiology
Date received: 1982-01-18
Decision date: 1982-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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