REBUILDER(TM)— 510(k) K874085

Substantially Equivalent

Micromed, Inc.

FDA 510(k) clearance K874085 for REBUILDER(TM), Substantially Equivalent on 1987-12-11. Applicant: Micromed, Inc.. Device class: 2.

Clearance details

Applicant: Micromed, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1987-10-07
Decision date: 1987-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Essex Junction, VT, 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.