KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD— 510(k) K902000

Name: FDA 510(k) clearance K902000
Creator: U.S. Food and Drug Administration
Published: 1990-08-21

Substantially Equivalent

Kevtek Medical Products, Inc.

FDA 510(k) clearance K902000 for KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD, Substantially Equivalent on 1990-08-21. Applicant: Kevtek Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Kevtek Medical Products, Inc.
Product code: Code FZS
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-05-02
Decision date: 1990-08-21
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.