LANTOR CUBE STERILIZER TEST PACK— 510(k) K882756

Substantially Equivalent

Lantor Group

FDA 510(k) clearance K882756 for LANTOR CUBE STERILIZER TEST PACK, Substantially Equivalent on 1988-10-06. Applicant: Lantor Group. Device class: 2.

Clearance details

Applicant: Lantor Group
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1988-07-05
Decision date: 1988-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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