PREEMICARE SERIES 4000 PHOTOTHERAPY LAMP— 510(k) K884133

Name: FDA 510(k) clearance K884133
Creator: U.S. Food and Drug Administration
Published: 1989-03-08

Substantially Equivalent

Preemicare Corp.

FDA 510(k) clearance K884133 for PREEMICARE SERIES 4000 PHOTOTHERAPY LAMP, Substantially Equivalent on 1989-03-08. Applicant: Preemicare Corp.. Device class: 2.

Clearance details

Applicant: Preemicare Corp.
Product code: Code LBI
Device class: Class 2
Regulation: 21 CFR 880.5700
Advisory panel: General Hospital
Date received: 1988-09-30
Decision date: 1989-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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