REPLICATION MEDICAL VESSEL GUARD— 510(k) K082782

Unknown

Replication Medical, Inc.

FDA 510(k) clearance K082782 for REPLICATION MEDICAL VESSEL GUARD, Unknown on 2009-04-02. Applicant: Replication Medical, Inc.. Device class: 2.

Clearance details

Applicant: Replication Medical, Inc.
Product code: Code OMR
Device class: Class 2
Regulation: 21 CFR 870.3470
Advisory panel: Cardiovascular
Date received: 2008-09-22
Decision date: 2009-04-02
Decision: Unknown
Clearance type: Traditional
Location: Alexandria, VA, 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.