Pioneer U601 Series Aspirator

FDA 510(k) K052650 · Merits Health Products Co., Ltd.

Substantially Equivalent

510(k) numberK052650

Submission

Device name
Pioneer U601 Series Aspirator
Applicant
Merits Health Products Co., Ltd.
Taichung, TW
Received
September 26, 2005
Decision date
November 4, 2005
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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 Pioneer U601 Series Aspirator cleared by the FDA?

Pioneer U601 Series Aspirator (K052650) received a 510(k) decision of Substantially Equivalent on November 4, 2005, 39 days after the submission was received.

What is the product code of K052650?

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