REMEDY MODEL 2Z12— 510(k) K012029

Substantially Equivalent

Apollo Corp.

FDA 510(k) clearance K012029 for REMEDY MODEL 2Z12, Substantially Equivalent on 2001-12-31. Applicant: Apollo Corp.. Device class: 2.

Clearance details

Applicant: Apollo Corp.
Product code: Code KMG
Device class: Class 2
Regulation: 21 CFR 880.6710
Advisory panel: General Hospital
Date received: 2001-06-28
Decision date: 2001-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, WI, 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.