SOMAVAC® 100 Sustained Vacuum System

FDA 510(k) K231063 · Somavac Medical Solutions, Inc.

Substantially Equivalent

510(k) numberK231063

Submission

Device name
SOMAVAC® 100 Sustained Vacuum System
Applicant
Somavac Medical Solutions, Inc.
Bartlett, TN, US
Received
April 14, 2023
Decision date
May 12, 2023
Decision
Substantially Equivalent (SESE)
Type
Special 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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More from Shenzhen Kingboom Technology Co., Ltd.

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Questions and answers

When was SOMAVAC® 100 Sustained Vacuum System cleared by the FDA?

SOMAVAC® 100 Sustained Vacuum System (K231063) received a 510(k) decision of Substantially Equivalent on May 12, 2023, 28 days after the submission was received.

What is the product code of K231063?

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