Vega Medical Suction Equipment, Model SU-01/SU-DC01

FDA 510(k) K102626 · Vega Technologies, Inc.

Substantially Equivalent

510(k) numberK102626

Submission

Device name
Vega Medical Suction Equipment, Model SU-01/SU-DC01
Applicant
Vega Technologies, Inc.
Taipei, TW
Received
September 13, 2010
Decision date
November 12, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JCX – Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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More from Taiwan Biomaterial Co., Ltd.

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Questions and answers

When was Vega Medical Suction Equipment, Model SU-01/SU-DC01 cleared by the FDA?

Vega Medical Suction Equipment, Model SU-01/SU-DC01 (K102626) received a 510(k) decision of Substantially Equivalent on November 12, 2010, 60 days after the submission was received.

What is the product code of K102626?

The FDA product code is JCX – Apparatus, Suction, Ward Use, Portable, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 878.4780.