TIDISHEILD— 510(k) K132953

Substantially Equivalent

Tidi Products,Llc

FDA 510(k) clearance K132953 for TIDISHEILD, Substantially Equivalent on 2014-02-18. Applicant: Tidi Products,Llc. Device class: 2.

Clearance details

Applicant: Tidi Products,Llc
Product code: Code PEM
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2013-09-20
Decision date: 2014-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Neenah, 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.