Creat Brand O-Rise General Aspirator

FDA 510(k) K873940 · Aesthetech Corp.

Substantially Equivalent

510(k) numberK873940

Submission

Device name
Creat Brand O-Rise General Aspirator
Applicant
Aesthetech Corp.
Paso Robles, CA, US
Received
September 28, 1987
Decision date
November 25, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K853189Creat Brand I/A Pack Creat Brand Phaco PackHQC · Traditional 09/24/1985SE
K843678Creat Brand Skin ExpanderLCJ · Traditional 11/06/1984SE
K841283Disposable Suction Tubing Set · Traditional 04/24/1984SE
K812210Creat Brand Wagner Chin ImplantFWP · Traditional 09/11/1981SE

Questions and answers

When was Creat Brand O-Rise General Aspirator cleared by the FDA?

Creat Brand O-Rise General Aspirator (K873940) received a 510(k) decision of Substantially Equivalent on November 25, 1987, 58 days after the submission was received.

What is the product code of K873940?

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