TRIPLEPLAY PRO— 510(k) K141360

Substantially Equivalent

Wildcat Medical, Inc.

FDA 510(k) clearance K141360 for TRIPLEPLAY PRO, Substantially Equivalent on 2014-06-12. Applicant: Wildcat Medical, Inc.. Device class: 2.

Clearance details

Applicant: Wildcat Medical, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-05-23
Decision date: 2014-06-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Tulsa, OK, US

Download summary PDF View on FDA.gov ↗

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