REVIVE SYSTEM— 510(k) K844445

Substantially Equivalent

Revive Systems Corp.

FDA 510(k) clearance K844445 for REVIVE SYSTEM, Substantially Equivalent on 1985-09-17. Applicant: Revive Systems Corp.. Device class: 2.

Clearance details

Applicant: Revive Systems Corp.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1984-11-16
Decision date: 1985-09-17
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.