Impact Model 323 Aspirator

FDA 510(k) K133196 · Impact Instrumentation, Inc.

Substantially Equivalent

510(k) numberK133196

Submission

Device name
Impact Model 323 Aspirator
Applicant
Impact Instrumentation, Inc.
West Caldwell, NJ, US
Received
October 17, 2013
Decision date
March 10, 2014
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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Questions and answers

When was Impact Model 323 Aspirator cleared by the FDA?

Impact Model 323 Aspirator (K133196) received a 510(k) decision of Substantially Equivalent on March 10, 2014, 144 days after the submission was received.

What is the product code of K133196?

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.