SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM— 510(k) K091720

Name: FDA 510(k) clearance K091720
Creator: U.S. Food and Drug Administration
Published: 2010-04-09

Substantially Equivalent

Sklar Corp.

FDA 510(k) clearance K091720 for SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM, Substantially Equivalent on 2010-04-09. Applicant: Sklar Corp.. Device class: 2.

Clearance details

Applicant: Sklar Corp.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2009-06-11
Decision date: 2010-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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