Thoraguard System

FDA 510(k) K181667 · Centese, Inc.

Substantially Equivalent

510(k) numberK181667

Submission

Device name
Thoraguard System
Applicant
Centese, Inc.
Omaha, NE, US
Received
June 25, 2018
Decision date
November 29, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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Questions and answers

When was Thoraguard System cleared by the FDA?

Thoraguard System (K181667) received a 510(k) decision of Substantially Equivalent on November 29, 2018, 157 days after the submission was received.

What is the product code of K181667?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.