Aspirator

FDA 510(k) K832274 · Wells Johnson Co.

Substantially Equivalent

510(k) numberK832274

Submission

Device name
Aspirator
Applicant
Wells Johnson Co.
Mchenry, IL, US
Received
July 12, 1983
Decision date
October 20, 1983
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.

510(k)DeviceDecision
K991437Wells Johnson Infusion System, Model 20-6000-00FRN · Traditional 08/30/1999SE
K984448Bircoll Balloon DissectorFZW · Traditional 01/28/1999SE
K971580Uas Ultrasonic Aspirator SystemLFL · Traditional 12/09/1997SE
K945876Weco Endoscopic System with Fiber Optic LightEQH · Traditional 12/04/1995SE
K945500Wells Johnson Fixation SystemJEY · Traditional 09/21/1995SE
K951519Weco Endoscopic System with Fiber Optic LightFWL · Traditional 06/14/1995SE
K945877Weco Endoscopic Systems with Fiber Optic LightHJM · Traditional 03/02/1995SE
K945805Wells Johnson Weco Monopolar/Frazier Suction ProbeGEI · Traditional 12/13/1994SE
K854068External Mechanical Fastener · Traditional 11/22/1985SE
K843188Wells Johnson Co. Chaj-Chir-Suction TipJOL · Traditional 09/20/1984SE

Questions and answers

When was Aspirator cleared by the FDA?

Aspirator (K832274) received a 510(k) decision of Substantially Equivalent on October 20, 1983, 100 days after the submission was received.

What is the product code of K832274?

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