PHOTOTHERAPY/PROCEDURE LAMP— 510(k) K771025

Substantially Equivalent

Cavitron Corp.

FDA 510(k) clearance K771025 for PHOTOTHERAPY/PROCEDURE LAMP, Substantially Equivalent on 1977-10-25. Applicant: Cavitron Corp.. Device class: 2.

Clearance details

Applicant
Cavitron Corp.
Product code
Code LBI
Device class
Class 2
Regulation
21 CFR 880.5700
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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