SENSITITRE ARIS MODULE— 510(k) K911419

Substantially Equivalent

Sensititre , Ltd.

FDA 510(k) clearance K911419 for SENSITITRE ARIS MODULE, Substantially Equivalent on 1992-07-01. Applicant: Sensititre , Ltd.. Device class: 2.

Clearance details

Applicant: Sensititre , Ltd.
Product code: Code LRG
Device class: Class 2
Regulation: 21 CFR 866.1640
Advisory panel: Microbiology
Date received: 1991-04-01
Decision date: 1992-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westlake, OH, US

Download summary PDF View on FDA.gov ↗

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