INTERCURE LTD. RESPI-LOW— 510(k) K000405

Substantially Equivalent

Intercure , Ltd.

FDA 510(k) clearance K000405 for INTERCURE LTD. RESPI-LOW, Substantially Equivalent on 2000-05-17. Applicant: Intercure , Ltd.. Device class: 2.

Clearance details

Applicant: Intercure , Ltd.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 2000-02-07
Decision date: 2000-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.