RESPERATE; MODEL RR-150— 510(k) K020399

Substantially Equivalent

Intercure , Ltd.

FDA 510(k) clearance K020399 for RESPERATE; MODEL RR-150, Substantially Equivalent on 2002-07-02. Applicant: Intercure , Ltd..

Clearance details

Applicant: Intercure , Ltd.
Product code: Code HCC
Advisory panel: Neurology
Date received: 2002-02-06
Decision date: 2002-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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